INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
Inventor
Sun, Roger
Deutsch, Eric
Abstract
The present invention relates to the use of a Lesion Progression Probability Score (LPPS) for predicting the risk of progression of a tumor lesion in a subject suffering from lung cancer when treated by immunotherapy, wherein the tumor lesion comprises a core tumoral region and a peritumoral region referred to as a ring and the LPPS of each lesion comprises 6 specific radiomics features. The invention also relates to the use of a patient progression probability score (PPPS) for predicting the risk of disease progression in a subject suffering from lung cancer when treated by immunotherapy, wherein the PPPS combines the LPPS values of all analyzed tumor lesions of the subject with a volume equal to or higher than a minimum volume Vmin. The invention also relates to therapeutic uses of immunotherapy in subjects with lung cancer with a low or moderate predicted risk of disease progression using the PPPS.
G16H 20/10 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients
G16H 30/40 - ICT specially adapted for the handling or processing of medical images for processing medical images, e.g. editing
G16H 50/30 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for calculating health indicesICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for individual health risk assessment
G16H 50/20 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
G16H 50/70 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for mining of medical data, e.g. analysing previous cases of other patients
2.
USE OF A RADIOMICS-BASED SIGNATURE FOR PREDICTING SURVIVAL AND/OR RESPONSE TO IMMUNOTHERAPY WITH OR WITHOUT PRELIMINARY LIVER FOCAL RADIOTHERAPY IN A SUBJECT WITH METASTATIC CANCER WITH LIVER METASTASIS
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
Inventor
Sun, Roger
Deutsch, Eric
Abstract
The present invention is in the field of cancer treatment. It relates to the use of a liver metastasis-specific radiomics-based signature for predicting in a subject suffering from a metastatic cancer with liver metastasis: (a) survival if treated by immunotherapy without preliminary liver focal radiotherapy, (b) response to immunotherapy without preliminary liver focal radiotherapy, (c) survival if treated by liver focal radiotherapy followed by immunotherapy, (d) response to liver focal radiotherapy followed by immunotherapy, or (e) any combination of (a) to (d). It further relates to a method for predicting any one of (a) to (e) based on the same liver metastasis-specific radiomics-based signature, as well as specific therapeutic uses of immunotherapy, with or without previous liver focal radiotherapy, in metastatic cancer subjects with liver metastasis, the selection of the specific treatment being made depending on the same liver metastasis-specific radiomics-based signature.
G16H 50/30 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for calculating health indicesICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for individual health risk assessment
G16H 30/20 - ICT specially adapted for the handling or processing of medical images for handling medical images, e.g. DICOM, HL7 or PACS
G16H 30/40 - ICT specially adapted for the handling or processing of medical images for processing medical images, e.g. editing
G16H 50/20 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
G16H 50/70 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for mining of medical data, e.g. analysing previous cases of other patients
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
A61B 5/06 - Devices, other than using radiation, for detecting or locating foreign bodies
INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
UNIVERSITÉ PARIS CITÉ (France)
INSTITUT GUSTAVE ROUSSY (France)
PARIS SCIENCES ET LETTRES (France)
FONDATION IMAGINE - INSTITUT DES MALADIES GENETIQUES (France)
ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS (France)
Inventor
Rodriguez, Raphaël
Muller, Sebastian
Cañeque, Tatiana
Colombeau, Ludovic
Thoidingjam, Leishemba Khuman
Côté, Francine
Abstract
The present invention relates to serotonin derivatives of general formula (I), and their use in the pharmaceutical field, in particular for preventing or treating metalloptosis associated disorders. The invention also relates to new serotonin derivatives of general formula (I) and their use for preventing or treating iron- and/or copper-associated disorders.
A61K 31/4045 - Indole-alkylaminesAmides thereof, e.g. serotonin, melatonin
A61K 31/454 - Non-condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
C07D 209/30 - IndolesHydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
C07D 401/06 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
C07D 403/06 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
C07D 405/12 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
C07D 405/14 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
4.
P21-ENGINEERED MONOCYTES AND RADIOTHERAPY IN SOLID TUMORS
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
Inventor
Perfettini, Jean-Luc
Allouch, Awatef
Abstract
The present invention concerns monocytes that over-express the cyclin-dependent kinase inhibitor p21 protein and therapeutic compositions comprising thereof, and in particular their use in the treatment of a mammal suffering from a solid cancer, preferably chosen from cancers resistant to radiation therapy and cancers sensitive to radiation therapy.
A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
A61K 38/17 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from animalsPeptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from humans
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
INSTITUT GUSTAVE ROUSSY (France)
Inventor
Taoufik, Yassine
De Goër De Herve, Marie-Ghislaine
Abstract
The present invention relates to a newly identified skin-tropic subset of Tscm that expresses the cutaneous homing marker CLA+. The identification of this new cell population of skin homing Tscm opens up new cell therapy strategies to treat cutaneous diseases, in particular cutaneous cancers such as Merkel cell carcinoma.
C12N 5/078 - Cells from blood or from the immune system
6.
METHOD FOR PERFORMING DIAGNOSIS, PROGNOSIS AND/OR THERAPEUTIC MONITORING OF DISEASES IMPACTING THE MINERAL PROFILE OF AT LEAST ONE BIOLOGICAL FLUID, AND A DEVICE, SYSTEM AND SOFTWARE PACKAGE USED TO IMPLEMENT SAME
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE LYON (France)
UNIVERSITE JEAN MONNET SAINT ETIENNE (France)
GCS INSTITUT DE CANCEROLOGIE STRASBOURG EUROPE (France)
CHU NANTES (France)
INSTITUT GUSTAVE ROUSSY (France)
HOSPICES CIVILS DE LYON (France)
UNIVERSITAT DES SAARLANDES (Germany)
Inventor
Tillement, Augustin
Tillement, Théodore
Tillement, Olivier
Lux, François
David, Laurent
Duroux, Coraline
Rossetti, Fabien
Decker, Yann
Fassbender, Klauss
Labrune, Elsa
Salle, Bruno
Deutsch, Eric
Morel, Daphné
Cassagnau, Philippe
Gillet, Philippe
Vourc’h, Mickael
Chevalier, Philippe
Pivot, Xavier
Detappe, Alexandre
Hagege, Agnes
Abstract
The aim of the invention is to provide an efficient, reliable and accurate method for performing diagnosis, prognosis and/or therapeutic monitoring of diseases impacting the mineral composition of at least one biological fluid. To this end, the method according to the invention essentially consists in - implementing at least one reference database (BDR) containing data relating, on the one hand, to samples of biological fluid, and, on the other hand, to the healthy or diseased subjects from which the samples of biological fluid were taken, these data comprising for each sample: (i) at least one mineral profile PM of concentrations of mineral elements in the biological fluid and (ii) conventional clinical data on the subjects; -implementing at least one sample Ex of biological fluid of at least one subject Sx to be tested; - analyzing each sample to determine at least one PM of Sx; - defining at least two categories with a view to making at least one prediction of membership of the subject Sx to be tested to at least one category of diagnosis (d), prognosis (p) and/or therapeutic monitoring (t), and, optionally to at least one subdivision of at least one category; - statistically processing the data of the BDR and displaying the processed data graphically, then positioning the data relating to Sx on this graphical display; - and/or carrying out AI-based machine learning using the data of the BDR; in order to make the prediction of membership regarding Sx and assist, by so doing, with the diagnosis, prognosis and/or therapeutic monitoring of diseases impacting the mineral composition of at least one biological fluid, for the subject Sx to be tested. The invention also relates to an electronic device, to a system for implementing the method, and to at least one computer program (and its medium) for executing the method.
G16H 10/40 - ICT specially adapted for the handling or processing of patient-related medical or healthcare data for data related to laboratory analysis, e.g. patient specimen analysis
G01N 33/50 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing
G16H 50/20 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
G16H 50/70 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for mining of medical data, e.g. analysing previous cases of other patients
7.
PRODUCTS AND USES THEREOF FOR PREDICTING THE SENSITIVITY OF A SUBJECT TO CANCER IMMUNOTHERAPY
INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (France)
ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS (France)
ECOLE NATIONALE SUPERIEURE DES MINES DE PARIS (France)
Inventor
Ginhoux, Florent
Gessain, Grégoire
Lerousseau, Marvin
Abstract
The present invention relates to the field of oncology. It more particularly relates to a method for evaluating the prognosis or the response to a therapeutic treatment of a subject having a squamous cell carcinoma by assessing the multinucleated giant cells status of a SCC tumor of the subject. This method may be advantageously computer-implemented for ease of use in the clinic.
INSERM (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE) (France)
UNIVERSITE PARIS- SACLAY (France)
Inventor
Goubet, Anne-Gaelle
Zitvogel, Laurence
Loriot, Yohann
Abstract
The present invention relates to the treatment of locally advanced and metastatic muscle-invasive bladder cancers (MIBC). The present invention provides compositions to be used in immunotherapy of MIBC, especially in combination with an anti-PD-1/PD-L1/PD-L2 antibody-based therapy. The present invention also provides biomarkers of response to anti-PD-1/PD-L1/PD-L2 immune checkpoint blocking antibodies (ICBs), alone or together with anti-CTLA4 antibodies and/or chemotherapy, for best guiding their neoadjuvant use and avoid unefficient administration of potentially toxic drugs to patients with localized bladder cancers.
The present invention relates to a liquid pharmaceutical composition comprising totally dissolved arsenic trioxide, at least one solubilizing agent selected from the metal-alkali acetates and metal-alkali lactates, and a solvent system which comprises a non-ionic surfactant and propylene glycol. The invention also relates to pharmaceutical capsule comprising the liquid composition of the invention. The invention further relates to said liquid pharmaceutical composition or said pharmaceutical capsule for use in the treatment of cancer or autoimmune diseases.
INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (France)
Inventor
Menger, Laurie
Abstract
The present invention relates to the field of oncology, in particular cellular therapy. The present invention more particularly relates to particular immune cells defective for ZNF217, products comprising such defective cells, and uses thereof.
C07K 14/47 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from animalsPeptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from humans from vertebrates from mammals
A61K 39/00 - Medicinal preparations containing antigens or antibodies
INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (France)
UNIVERSITÉ PARIS CITÉ (France)
SORBONNE UNIVERSITÉ (France)
ASSISTANCE PUBLIQUE-HÔPITAUX DE PARIS (APHP) (France)
UNIVERSITÉ PARIS-SACLAY (France)
INSTITUT GUSTAVE ROUSSY (France)
Inventor
Lambertucci, Flavia
Pan, Hui
Martins, Isabelle
Kroemer, Guido
Nogueira Recalde, Uxia
Kepp, Oliver
Abstract
The present disclosure provides improved methods, therapeutic regimens, and systems for treating a disease associated with a pituitary malignancy in a subject, such as treating Cushing Syndrome, or treating one or more symptoms of Cushing Syndrome in subjects, through the inhibition of extracellular diazepam binding inhibitor (DBI) by various methods. The present disclosure also relates to compositions for use and methods in treating synovial inflammation in a subject, the compositions for use and methods comprising an agent that reduces human diazepam binding inhibitor (DBI) activity or expression. The present disclosure also relates to compositions for use and methods in treating degenerative joint disease, joint inflammation, and manifestations thereof in a subject, the compositions for use and methods comprising an agent that reduces human diazepam binding inhibitor (DBI) activity or expression.
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
Inventor
Benzazon, Nathan
De Kermenguy, François
Deutsch, Eric
Robert, Charlotte
Diallo, Ibrahima
Abstract
The present invention relates to a method for determining the irradiation dose that has been or will be received by a lymphocyte L during a radiotherapy treatment performed on a target organ of a patient, said method comprising the steps of: a) collecting the following data associated to said radiotherapy treatment: - the radiation treatment planning applied to or scheduled for said patient, - the radiation reference doses applied to or scheduled for said patient, and - the number, location and volume of the lymphoid organs that have been or will be irradiated (if any), b) simulating the lymphocyte path between the several organs of the body, c) determining the irradiation dose received by said lymphocyte L during said radiotherapy treatment would it be circulating in peripheral blood, or present in or circulating between lymphoid organs, d) optionally, determining the irradiation dose received by at least one out-of-field lymphoid organ during said radiotherapy treatment, e) combining these data in order to determine the irradiation dose that has been or will be received by the lymphocytes of said patient during said radiotherapy treatment.
G16H 20/40 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to mechanical, radiation or invasive therapies, e.g. surgery, laser therapy, dialysis or acupuncture
13.
Treating Chronic Myelomonocytic Leukemia with CXCL8 Receptor Inhibitors
Institut National de la Sante et de la Recherche Medicale (INSERM) (France)
Inventor
Selimoglu-Buet, Dorothee
Solary, Eric
Willekens, Christophe
Abstract
A method for treating chronic myelomonocytic leukemia (CMML), or for maintaining or enhancing the proliferation of wildtype hematopoietic stem cells in patients suffering from CMML, by administering to a patient in need thereof a pharmaceutical composition containing an effective amount of an inhibitor of the CXCL8 receptor.
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT GUSTAVE ROUSSY (France)
UNIVERSITE PARIS-SACLAY (France)
INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (France)
VIROXIS (France)
Inventor
Dupressoir, Anne
Tran, Ngoc Huong Giang
Heidmann, Thierry
Abstract
The invention concerns new oncolytic viruses and their uses In particular, the invention is a viral particle for its use in the prevention and/or the treatment of a tumor, said viral particle comprising: an inactivated nucleic acid sequence encoding the native envelope glycoprotein of the IROV encoded by said IROV genome; and a nucleic acid sequence encoding a retroviral envelope glycoprotein or a fragment thereof having a native targeting capacity for said host cell surface protein.
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
Inventor
Bigenwald, Camille
Daillere, Romain
Zitvogel, Laurence
Abstract
The present invention is based on the demonstration that bacteria of the Akkermansia genus improve the response to CAR T-cells therapy. According to the invention, Akkermansia bacteria are administered to patients treated with CAR T-cells, especially if their gut microbiome was devoid of such bacteria before administering said CAR T-cells.
PRODUCTS AND USES THEREOF FOR PREDICTING THE SENSITIVITY OF A SUBJECT TO CANCER IMMUNOTHERAPY INVOLVING AN ANTI-PD(L)1 AND AN ANTI-ANGIOGENIC AGENT, AND FOR SELECTING OPTIMIZED THERAPY
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
Inventor
Danlos, François-Xavier
Marabelle, Aurélien
Mouraud, Séverine
Chaput-Gras, Nathalie
Tselikas, Lambros
Job, Bastien
Abstract
The present invention relates to a method of predicting assessing or monitoring the sensitivity of a subject having a cancer to a combination therapy, preferably to a therapy combining an immunotherapeutic agent and an anti-angiogenic agent, and to corresponding kits and uses thereof. The method of predicting, assessing or monitoring the sensitivity of a subject having a cancer or malignant tumor to a proposed combination therapy typically comprises a step a) of determining, in a biological sample from said subject, the presence, absence or expression level or proportion of at least one biomarker, for example at least two biomarkers, and when the expression level or proportion is determined a step b) of comparing said expression level or proportion to reference expression level(s) or to reference expression ratio(s), thereby predicting, assessing or monitoring whether the subject having a tumor is responsive or resistant to the proposed combination therapy.
G01N 33/574 - ImmunoassayBiospecific binding assayMaterials therefor for cancer
G01N 33/50 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing
G01N 33/68 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving proteins, peptides or amino acids
G01N 33/74 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving hormones
17.
METHOD FOR PROCESSING AT LEAST A PRE-CONTRAST IMAGE AND A CONTRAST IMAGE RESPECTIVELY DEPICTING A BODY PART PRIOR TO AND AFTER AN INJECTION OF A FIRST DOSE OF CONTRAST AGENT
The present invention relates to method for medical imaging, the method being characterized in that it comprises the implementation, by a data processor (11b) of a second server (1b), of steps of: (a) Obtaining at least one candidate pre-contrast image and a candidate contrast image respectively depicting a body part prior to and after an injection of a first dose of contrast agent, wherein said first dose is higher than a predetermined low dose, the predetermined reduced dose being lower than a predetermined standard dose; a convolutional neural network, CNN, being trained to reconstruct, from at least a pre-contrast input image and a low dose contrast input image respectively depicting a body part prior to and after an injection of said low dose of contrast agent, a standard dose contrast image depicting said body part after an injection of said standard dose of contrast agent; (b) Simulating an injection of a second dose of contrast agent which is higher than the standard dose, wherein said simulating comprises generating a synthetic contrast image by applying the CNN to the at least one candidate pre-contrast image and the candidate contrast image.
INSERM (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE) (France)
INSTITUT GUSTAVE ROUSSY (France)
Inventor
Taoufik, Yassine
De Goër De Herve, Marie-Ghislaine Madeleine
Abstract
The present invention relates to a new and specific T-cell therapy strategy based on the use of memory stem T-cells (Tscm), in particular highly functional memory stem T-cells (Tscm) negatively selected on the basis of inhibitory receptor expression. This new cellular immunotherapy may be applied to PML patients but also to other infections or cancers for which the specific memory T cell responses are functionally impaired.
The present invention relates to a method of predicting, assessing or monitoring the sensitivity of a subject having a cancer to an immunotherapy, preferably to an immunotherapy combining at least two immunotherapeutic agents, and to corresponding kits and uses thereof. The method of predicting, assessing or monitoring the sensitivity of a subject having a tumor to an immunotherapy typically comprises a step of assessing, before any immunotherapeutic treatment step in the subject, the presence of CD4+CD25highCD39high T cells in a tumor sample of the subject, the presence of CD4+CD25highCD39high T cells in the tumor sample of the subject being indicative of sensitivity of the subject to the immunotherapy, and the absence of CD4+CD25highCD39high T cells in the tumor sample of the subject being indicative of resistance of the subject to the immunotherapy.
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
NANOH (France)
PALLADIN INSTITUTE OF BIOCHEMISTRY, NATIONAL ACADEMY OF SCIENCES OF UKRAINE (Ukraine)
Inventor
Morel, Daphné
Deutsch, Eric
Tillement, Olivier
Lux, François
David, Laurent
Rossetti, Fabien
Durand, Arthur
Howard, Jordyn
Rosson, Elise
Komisarenko, Serhiy
Borisova, Tatiana
Lysenko, Volodymyn
Tillement, Augustin
Abstract
The present disclosure relates to methods for treating radioactive contamination, in particular internal radioactive contamination, said method comprising orally administering, in a subject at risk or suspected of radioactive contamination, an efficient amount of a functionalized polymer, wherein said functionalized polymer is a specific statistic chitosan polymer wherein a part of the monomeric units are functionalized with a chelating moiety which complexes said radionuclide.
A61K 47/61 - Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additivesTargeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule the organic macromolecular compound being a polysaccharide or a derivative thereof
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
UNIVERSITE PARIS-SACLAY (France)
Inventor
Susini, Sandrine
Tselikas, Lambros
Marabelle, Aurélien
Martineau, Romane
Abstract
The present invention relates to a new drug conjugate comprising a CTLA4 targeting molecule, at least one cytotoxic agent, and a linker connecting the CTLA4 targeting molecule and the cytotoxic agent, as well as to compositions and kits comprising such a drug conjugate, and to uses thereof in particular for treating cancer and/or for preventing a cancer relapse in a subject in need thereof.
A61K 47/68 - Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additivesTargeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
C07K 16/28 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
A61K 39/00 - Medicinal preparations containing antigens or antibodies
22.
BIOLOGICAL MARKER OF INTESTINAL DYSBIOSIS, USEFUL FOR PREDICTING THE RESPONSE OF A CANCER PATIENT TO AN ANTI-PDI DRUG
The present invention relates to the field of anticancer treatment. In particular, the present invention concerns the role of the gut microbiota in the efficacy of immune checkpoints inhibitors (ICI)-based treatments and provides methods for determining if a patient is likely to benefit from an ICI-based treatment, more precisely, treatment comprising administration of an antibody directed against PD1 or PD-L1. The present invention provides a method for stratifying cancer patients according to their potential need of bacterial complementation before receiving an ICI-based treatment. The present invention also provides a simple method for determining whether an individual has an intestinal dysbiosis.
C12Q 1/689 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for detection or identification of organisms for bacteria
23.
METHODS FOR THE TREATMENT OF ANAPLASTIC LARGE CELL LYMPHOMA
INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (France)
FONDATION IMAGINE (France)
INSTUTUT GUSTAVE ROUSSY (France)
UNIVERSITÉ PARIS CITE (France)
UNIVERSITÉ PARIS-SACLAY (France)
UNIVERSITÉ TOULOUSE III - PAUL SABATIER (France)
ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS (France)
CENTRE HOSPTIALIER UNIVERSITAIRE DE TOULOUSE (France)
Inventor
Causse Brunet, Erika
Mercher, Thomas
Babin, Loélia
Robert, Elie
Darchen, Alice
Lamant, Laurence
Meggetto-Pradelle, Fabienne
Abstract
Anaplastic large cell lymphoma (ALCL) is a rare and aggressive peripheral T-cell lymphoma affects lymph nodes and extra-nodal sites with characteristic skin lesions. Approximatively half of the tumors express the NPM1-ALK fusion from the translocation t(2;5)(p23;q32). In the present study, the inventors identify ROR2 as progressively up regulated thought tumorigenesis. Patient samples show a significantly high ROR2 expression (transcriptomic data) as well as a strong ROR2 protein expression (IHC) with some tumors displaying a clear membrane signal. ROR2 mRNA expression level is also positively correlated to NPM-ALK expression level in tumor cells and is not expressed in normal T cells. In addition, ROR2 protein level is significantly increased in resistant cells to the ALK inhibitor, crizotinib, used in clinical trials for children with refractory tumors. This result opens the road to ROR2 specific therapies: ROR2 inhibitors, monoclonal antibodies therapies or even ROR2 specific CAR cells, including for ALCL ALK(+) resistant tumors.
C07K 16/28 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
24.
COMBINATION THERAPY FOR TREATING TUMORS WITH RADIOTHERAPY
INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (France)
INSTITUT GUSTAVE ROUSSY (France)
Inventor
Perfettini, Jean-Luc
Le Duc, Géraldine
De Beaumont, Olivier
Tannous, Désirée
Abstract
The disclosure relates to a method of treating cancer in a subject in need thereof, said method comprising (i) a priming phase, and (ii) a treatment phase, wherein said priming phase comprises administering an efficient amount of said nanoparticles in combination with a low-dose radiotherapy, and said treatment phase comprises administering an efficient amount of said nanoparticles in combination with radiotherapy, optionally in combination with an immune checkpoint blocker, wherein said nanoparticles are nanoparticles containing an element with an atomic Z number higher than 20, preferably higher than 50, for example between 40 and 83, more preferably gadolinium or bismuth.
A61K 41/00 - Medicinal preparations obtained by treating materials with wave energy or particle radiation
A61K 47/69 - Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additivesTargeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
Centre National de la Recherche Scientifique (France)
INSTITUT GUSTAVE ROUSSY (France)
Institut National de la Santé et de la Recherche Médicale (France)
Institut Curie (France)
Université Paris Cité (France)
Inventor
Rodriguez, Raphaël
Cote, Francine
Coman, Tereza
Debieu, Sylvain
Caneque Cobo, Tatiana
Hermine, Olivier
Muller, Sebastian
Falabregue, Marion
Abstract
The present invention relates to novel serotonin derivatives of formula (I):
The present invention relates to novel serotonin derivatives of formula (I):
The present invention relates to novel serotonin derivatives of formula (I):
or a pharmaceutically acceptable salt and/or solvate thereof.
The present invention relates to novel serotonin derivatives of formula (I):
or a pharmaceutically acceptable salt and/or solvate thereof.
Another object of the present invention relates to the use of compound of formula (I) as a drug, in particular in the prevention and/or the treatment of iron overload-associated disorders.
A61P 25/28 - Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
C07D 405/12 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
26.
T CELL IMMUNOTHERAPY DERIVED FROM AUTOLOGOUS STEM CELL MEMORY T CELLS
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
INSTITUT GUSTAVE ROUSSY (France)
Inventor
Taoufik, Yassine
De Goër De Herve, Marie-Ghislaine Madeleine
Abstract
The present invention relates to a new and specific T-cell therapy strategy based on the use of memory stem T-cells (Tscm). This new cellular immunotherapy may be applied to PML patients but also to other infections or cancers for which the specific memory T cell responses are functionally impaired.
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
Inventor
Blériot, Camille
Ginhoux, Florent
Abstract
The invention pertains to isolated population of tumor-associated macrophage cell populations, their use in prognosing the malignancy and the outcome of solid tumors, as well as compounds which inhibit the expression of certain genes in these macrophage cells, in tumor-associated macrophage populations, for use for treating a solid cancer in a subject in need thereof.
INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (France)
UNIVERSITÉ PARIS CITÉ (France)
SORBONNE UNIVERSITÉ (France)
ASSISTANCE PUBLIQUE-HÔPITAUX DE PARIS (APHP) (France)
INSTITUT GUSTAVE ROUSSY (France)
Inventor
De Boer, Mark
Kroemer, Guido
Montegut, Léa
Martins, Isabelle
Pan, Hui
Chen, Hui
Li, Sijing
Abstract
The present disclosure provides improved methods, compositions, agents, therapeutic regimens, and systems for cancer treatment, such as improving the outcome of chemo- and/or immunotherapies, and/or inducing autophagy in subjects through the inhibition of extracellular diazepam binding inhibitor (DBI) by various methods.
A61K 31/573 - Compounds containing cyclopenta[a]hydrophenanthrene ring systemsDerivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
C07K 16/44 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material not provided for elsewhere
A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
A liquid pharmaceutical composition comprising an aqueous solvent, nicotinamide and at least one imipridone derivative of formula (I). A process for manufacturing said liquid pharmaceutical composition, wherein the process comprises the steps of (a) Dissolving nicotinamide in an aqueous solvent, preferably water; (b) Adding at least one pH modifier and at least one imipridone derivative to the solution obtained in step (a); and (c) Optionally sterilizing the solution obtained in step (b). A 1: 1 imipridone derivative nicotinamide complex or cocrystal, wherein the imipridone derivative is of formula (I). Said compositions for use in the treatment of cancer.
INSTITUE OF CANCER RESEARCH ROYAL CANCER HOSPITAL (United Kingdom)
INSTITUT GUSTAVE ROUSSY (France)
UNIVERSITÉ PARIS-SACLAY (France)
INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (INSERM) (France)
Inventor
Lord, Christopher
Chabanon, Roman
Postel-Vinay, Sophie
Abstract
The present invention relates to adenosine deaminase 1 (ADAR1) inhibitors for use in a method of treating an individual with a homologous recombination defective (HRD) cancer, as well as methods for selecting individuals suitable for such treatments.
C12Q 1/6886 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
G01N 33/50 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing
31.
METHOD FOR IDENTIFYING HARD-TO-TREAT OSTEOSARCOMA PATIENTS AT DIAGNOSIS AND IMPROVING THEIR OUTCOME BY PROVIDING NEW THERAPY
The present invention provides tools for stratifying patients suffering from osteosarcoma, in order to identify patients having poor prognosis tumors. The invention also pertains to the use of an inhibitor of the PPARγ pathway as an antineoplastic treatment to improve the overall survival of patients with a poor prognosis osteosarcoma.
C12Q 1/6886 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
A61K 31/4409 - Non-condensed pyridinesHydrogenated derivatives thereof only substituted in position 4, e.g. isoniazid, iproniazid
INSERM (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE) (France)
Inventor
Fidelle, Marine
Zitvogel, Laurence
Daillere, Romain
Rauber, Conrad
Abstract
The present invention relates to the field of anticancer immunotherapy. In particular, the present invention concerns the role of the MAdCAM-1/α4β7 axis the gut microbiota in the efficacy of cancer treatments and provides methods for determining if a patient is likely to benefit from a cancer treatment, more precisely, and immuno-oncology (I-O) therapy, such as a treatment comprising administration of an antibody directed against immune checkpoint blockers PD1, PD-L1 or PD-L2 alone or together with CTLA4 and/or chemotherapy. The present invention also provides methods to improve the efficacy of such a treatment in patients in need thereof.
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (France)
INSTITUT GUSTAVE ROUSSY (France)
Inventor
Brenner, Catherine
Taran, Frédéric
Cintrat, Jean-Christophe
Perfettini, Jean-Luc
Abstract
The invention relates to compounds capable of inducing autophagy and metabolic reprogramming and to the use thereof as cardioprotectors, in particular in the context of anticancer therapy.
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
UNIVERSITE PARIS-SACLAY (France)
Inventor
Derosa, Lisa
Iebba, Valerio
Zitvogel, Laurence
Abstract
The present invention relates to a score (TOPOSCORE) for describing eubiosis or dysbiosis in an individual, that can be used, inter alia, for determining if a patient is likely to respond to an immune-oncology treatment, more precisely, a treatment comprising administration of an immune checkpoint inhibitor (ICI). The TOPOSCORE represents a robust biomarker predicting immunosensitivity and immunoresistance to ICI on an individual basis.
A method implemented by computer means for training a decision system for segmenting medical images from a training set of annotated medical images, the segments belonging to at least one class, each annotation of the medical images including quantitative information about a number of pixels of the image that belongs to each of the classes, the method using weakly-supervised algorithm based on a percentage of the pixels of the image belonging to a concerned class.
09 - Scientific and electric apparatus and instruments
16 - Paper, cardboard and goods made from these materials
26 - Small items for dressmaking; artifical flowers; false hair
35 - Advertising and business services
36 - Financial, insurance and real estate services
41 - Education, entertainment, sporting and cultural services
Goods & Services
Media for recording, transmitting, reproducing and
duplicating sound, data or images; data media [electric or
electronic]; pre-recorded or blank video cassettes and video
disks, pre-recorded or blank laser cassettes and laser
discs, magnetic tape cassettes and sound recording discs,
sound and audiovisual recordings; audio digital compact
disks, video disks, optical disks; magnetic cards; memory
cards or integrated circuit cards; magnetic and electronic
pens; computer programs, software on all types of material
carriers, software for generating virtual images, databases,
text and sound data banks, image banks; data downloadable on
a computer or a portable telephone and particularly
ringtones, sounds, music, photographs, videos, images,
logos, texts and any other content; electronic publications
and downloadable electronic publications particularly via an
international telecommunication network; Downloadable
digital files authenticated by non-fungible tokens [NFTs]. Printing products (printed matter); bookbinding material;
photographs; stationery; instructional or teaching material
(except apparatus); writing or drawing books; notepads;
notebooks; printing blocks; paper; cardboard; boxes of
cardboard or paper; pens and pen refills, pencils; pencil
sharpeners; posters; posters; printed matter; albums; cards;
writing paper; files; folders for papers; labels, not of
textile; stickers and transfers [decalcomanias]; drawing
pads; books; newspapers and periodicals; handouts;
magazines; journals (magazines); publications; atlases;
newsletters; catalogs; prospectuses; pamphlets; calendars;
diaries (planners); writing instruments; drawings; face
towels of paper; bags and small bags (envelopes, pouches) of
paper or plastic for packaging; specialized journals in the
medical field. Ribbons and braid, pins; ornamental novelty badges; hair
bands; brassards; competitors' numbers; elastic ribbons. Advertising; dissemination of advertising material
(leaflets, prospectuses, printed matter, samples, free
CD-ROMs); rental of advertising space, updating of
advertising documents; dissemination of advertisements,
media planning services; subscription to a telephone
information services; subscriptions to a global
telecommunications network (the Internet) or a private
access network (intranet); subscription services to a
multimedia or database server center; subscription service
to a database; subscriptions to electronic newspapers;
newspaper subscription services for others; administrative
management of a platform for hosting and exchanging data,
images, sounds, sound and/or video recordings, videos;
administrative management of a database on the Internet;
services for inputting, editing, compiling and processing
data and more generally for recording, transcribing and
systematizing written communications and sound and/or image
recordings; collection and systematization of data in a
central file; data search in computer files for others;
assistance and business management assistance for
non-commercial entities; computer file management for
others; recording, composition, systematization of data
written or received by computer, and particularly data
communication or remote computing; public relations;
organization of trade fairs and exhibitions for advertising
purposes; organization of competitions in connection with
advertising; online advertising on a computer network;
administrative management on behalf of non-commercial
entities, including organizations and foundations; business
assistance and management and administrative services,
namely, advice, information and inquiries for the management
of non-commercial entities, including associations and
foundations, management assistance for associations and
foundations; consulting, information or inquiries in
connection with associations in the conduct of their
activities, namely consulting, information or inquiries for
associations in the field of administration and accounting;
conducting of online virtual trade fairs; networking
services with bloggers; advertising and marketing services
provided by means of blogging; retail service for
downloadable digital files authenticated by non-fungible
tokens [NFTs]. Investing and managing funds; financing services for the
publication and transmission of information relating to
science, medicine, in particular for medical research;
financial consultancy for projects in the field of science
and medicine, particularly for medical research; charitable
fundraising; mutual funds; collection and distribution of
donations for business associations and companies; funding
studies and evaluations in the field of patronage; raising
capital; financial transactions; sponsorship and financial
assistance to and from companies, associations,
non-governmental organizations or special programs in
particular in the field of medical research; advice,
information or inquiries to associations on financial
matters and fiscal valuations. Education; training; sporting and cultural activities;
information relating to entertainment or education;
publication of books; videotape film production;
organization of competitions (education or entertainment);
organization and conducting of colloquiums, conferences or
congresses; organization of exhibitions for cultural or
educational purposes; organization and conducting of award
ceremonies, concerts, fashion shows, charity galas;
production and organization of shows; booking of theater
halls; education and entertainment; organization of
information campaigns (for cultural or educational purposes)
or professional or other events (excluding commercial or
advertising events); organization and conducting of training
workshops, practical training, editing and publishing of
books and any kind of sound and/or visual media, recording,
transmission and reproduction of sound and/or images (except
advertising matter); editing and publishing of multimedia
carriers; book lending; electronic publication of
downloadable and non-downloadable books and periodicals
online; publishing of texts, illustrations, newspapers,
magazines, periodicals and more generally of all
publications other than advertising texts, including
electronic and digital publications, including electronic
and digital books; correspondence courses; film production,
video production; advice, information or inquiries to
associations on culture and art matters; editing of medical
publications; publication of scientific articles relating to
medical technology; organization of conferences and
symposiums in the field of medical science; provision of
online training seminars; providing online colloquiums,
conferences or congresses, exhibitions for cultural or
educational purposes; entertainment services, namely,
providing virtual environments in which users can interact
for recreational, leisure or entertainment purposes;
entertainment services, namely, organization and hosting of
virtual shows and social entertainment events.
37.
CD207 DENDRITIC CELLS AS A BIOMARKER FOR TUMOURAL PROGRESSION AND THERAPEUTIC TARGET
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
UNIVERSITE PARIS-SACLAY (France)
Inventor
Ginhoux, Florent
Dutertre, Charles-Antoine
Abstract
The present invention proposes an efficient method to prognose the evolution of a solid cancer in a subject in need thereof, by analysing the frequency of a particular subset of dendritic cells as well as their relative number as compared to that of another subset of dendritic cells in a tumour sample of said subject. More precisely, the method of the invention comprises the step of detecting and quantifying the frequency of CD207+conventional dendritic cells of type 2 and 3 ("CD207+DC2+DC3") in a tumour sample of said subject. If the frequency of said cells is high, in particular in the tumour core, then it means that the subject has a bad prognosis. The method of the invention also comprises the calculation within the tumour of the ratio of the number of conventional dendritic cells of type 1 (cDC1) to the number of CD207+DC2+DC3 to predict T-cell clonality in the tumour. As a matter of fact, the inventors herein establish that the CD207+DC2+DC3 participate in the regulation of the anti-tumour T-cell cytotoxicity by limiting T-cell clonality and impairing the CD8+tissue resident memory T cell (TRM) response. Their analysis furthermore reveals that the CD207+ DC2+DC3 are enriched in biopsies from later deceased patients as compared to alive patients suffering from different solid cancers. The inventors also propose to reduce the abundance of these cells within the tumour core, e.g., by appropriate drugs, in order to limit the development of said solid tumour in the subject.
G01N 33/574 - ImmunoassayBiospecific binding assayMaterials therefor for cancer
C12Q 1/6886 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
C07K 16/28 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
A61K 39/00 - Medicinal preparations containing antigens or antibodies
38.
MOBILISATION CANCER Tous ensemble avec les chercheurs. Fondation ARC pour la recherche sur le cancer Gustave Roussy cancer campus Grand Paris
09 - Scientific and electric apparatus and instruments
16 - Paper, cardboard and goods made from these materials
26 - Small items for dressmaking; artifical flowers; false hair
35 - Advertising and business services
36 - Financial, insurance and real estate services
41 - Education, entertainment, sporting and cultural services
Goods & Services
Media for recording, transmitting, reproducing and
duplicating sound, data or images; data media [electric or
electronic]; pre-recorded or blank video cassettes and video
disks, pre-recorded or blank laser cassettes and laser
discs, magnetic tape cassettes and sound recording discs,
sound and audiovisual recordings; audio digital compact
disks, video disks, optical disks; magnetic cards; memory
cards or integrated circuit cards; magnetic and electronic
pens; computer programs, software on all types of material
carriers, software for generating virtual images, databases,
text and sound data banks, image banks; data downloadable on
a computer or a portable telephone and particularly
ringtones, sounds, music, photographs, videos, images,
logos, texts and any other content; electronic publications
and downloadable electronic publications particularly via an
international telecommunication network; downloadable
digital files authenticated by non-fungible tokens [NFTs]. Printing products (printed matter); bookbinding material;
photographs; stationery; instructional or teaching material
(except apparatus); writing or drawing books; notepads;
notebooks; printing blocks; paper; cardboard; boxes of
cardboard or paper; pens and pen refills, pencils; pencil
sharpeners; posters; posters; printed matter; albums; cards;
writing paper; files; folders for papers; labels, not of
textile; stickers and transfers [decalcomanias]; drawing
pads; books; newspapers and periodicals; handouts;
magazines; journals (magazines); publications; atlases;
newsletters; catalogs; prospectuses; pamphlets; calendars;
diaries (planners); writing instruments; drawings; face
towels of paper; bags and small bags (envelopes, pouches) of
paper or plastic for packaging; specialized journals in the
medical field. Ribbons and braid, pins; ornamental novelty badges; hair
bands; brassards; competitors' numbers; elastic ribbons. Advertising; dissemination of advertising material
(leaflets, prospectuses, printed matter, samples, free
CD-ROMs); rental of advertising space, updating of
advertising documents; dissemination of advertisements,
media planning services; subscription to a telephone
information services; subscriptions to a global
telecommunications network (the Internet) or a private
access network (intranet); subscription services to a
multimedia or database server center; subscription service
to a database; subscriptions to electronic newspapers;
newspaper subscription services for others; administrative
management of a platform for hosting and exchanging data,
images, sounds, sound and/or video recordings, videos;
administrative management of a database on the Internet;
services for inputting, editing, compiling and processing
data and more generally for recording, transcribing and
systematizing written communications and sound and/or image
recordings; collection and systematization of data in a
central file; data search in computer files for others;
assistance and business management assistance for
non-commercial entities; computer file management for
others; recording, composition, systematization of data
written or received by computer, and particularly data
communication or remote computing; public relations;
organization of trade fairs and exhibitions for advertising
purposes; organization of competitions in connection with
advertising; online advertising on a computer network;
administrative management on behalf of non-commercial
entities, including organizations and foundations; business
assistance and management and administrative services,
namely, advice, information and inquiries for the management
of non-commercial entities, including associations and
foundations, management assistance for associations and
foundations; consulting, information or inquiries in
connection with associations in the conduct of their
activities, namely consulting, information or inquiries for
associations in the field of administration and accounting;
conducting of online virtual trade fairs; networking
services with bloggers; advertising and marketing services
provided by means of blogging; retail service for
downloadable digital files authenticated by non-fungible
tokens [NFTs]. Investing and managing funds; financing services for the
publication and transmission of information relating to
science, medicine, in particular for medical research;
financial consultancy for projects in the field of science
and medicine, particularly for medical research; charitable
fundraising; mutual funds; collection and distribution of
donations for business associations and companies; funding
studies and evaluations in the field of patronage; raising
capital; financial transactions; sponsorship and financial
assistance to and from companies, associations,
non-governmental organizations or special programs in
particular in the field of medical research; advice,
information or inquiries to associations on financial
matters and fiscal valuations. Education; training; sporting and cultural activities;
information relating to entertainment or education;
publication of books; videotape film production;
organization of competitions (education or entertainment);
organization and conducting of colloquiums, conferences or
congresses; organization of exhibitions for cultural or
educational purposes; organization and conducting of award
ceremonies, concerts, fashion shows, charity galas;
production and organization of shows; booking of theater
halls; education and entertainment; organization of
information campaigns (for cultural or educational purposes)
or professional or other events (excluding commercial or
advertising events); organization and conducting of training
workshops, practical training, editing and publishing of
books and any kind of sound and/or visual media, recording,
transmission and reproduction of sound and/or images (except
advertising matter); editing and publishing of multimedia
carriers; book lending; electronic publication of
downloadable and non-downloadable books and periodicals
online; publishing of texts, illustrations, newspapers,
magazines, periodicals and more generally of all
publications other than advertising texts, including
electronic and digital publications, including electronic
and digital books; correspondence courses; film production,
video production; advice, information or inquiries to
associations on culture and art matters; editing of medical
publications; publication of scientific articles relating to
medical technology; organization of conferences and
symposiums in the field of medical science; provision of
online training seminars; providing online colloquiums,
conferences or congresses, exhibitions for cultural or
educational purposes; entertainment services, namely,
providing virtual environments in which users can interact
for recreational, leisure or entertainment purposes;
entertainment services, namely, organization and hosting of
virtual shows and social entertainment events.
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
Inventor
Annereau, Maxime
Dowek, Antoine
Legrand, François-Xavier
Rieutord, André
Abstract
The invention provides a pharmaceutical composition in oral liquid form, comprising vinorelbine, or a pharmaceutically acceptable salt thereof, and a cyclodextrin that is sulfobutylether-beta-cyclodextrin (SBE-beta-CD), preferably wherein at least 95%, vinorelbine, or said pharmaceutically acceptable salt thereof, is in form of an inclusion complex with said cyclodextrin.
A61K 47/69 - Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additivesTargeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
Inventor
Morel, Daphné
Deutsch, Eric
Tillement, Olivier
Lux, François
David, Laurent
Rossetti, Fabien
Durand, Arthur
Howard, Jordyn
Rosson, Elise
Abstract
The present disclosure relates to a functionalized polymer, for use in treating a disease correlated with heavy metal-induced toxicity or heavy metal-induced carcinogenicity in a subject in need thereof, wherein said functionalized polymer is soluble in aqueous solution, has a weight average molecular mass between 30 kDa and 5000 kDa, and wherein a part of the monomeric units are functionalized with a chelating moiety, wherein therapeutically efficient amount of said functionalized polymer is administered orally to the subject.
A61K 31/715 - Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkagesDerivatives thereof, e.g. ethers, esters
A61K 31/718 - Starch or degraded starch, e.g. amylose, amylopectin
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITÉ PARIS CITÉ (France)
SORBONNE UNIVERSITÉ (France)
ASSISTANCE PUBLIQUE-HÔPITAUX DE PARIS (APHP) (France)
UNIVERSITÉ PARIS-SACLAY (France)
INSTITUT GUSTAVE ROUSSY (France)
Inventor
Kroemer, Guido
Abdellatif, Mahmoud
Montégut, Léa
Martins, Isabelle
Abstract
Cardiomyopathies are heart muscle disorders which represent a heterogeneous group of diseases that often lead to progressive heart failure with significant morbidity and mortality. Here, the inventors show that neutralization of acyl CoA binding protein (ACBP)/diazepam binding inhibitor (DBI) reduces the deleterious effect of the anthracycline doxorubicin on cardiac function. Since anthracycline-induced heart failure and anthracycline-induced senescence are models of accelerated cardiac aging, it is also plausible to use ACBP/DBI inhibition or neutralization as a method to prevent or treat aging of the cardiovascular system. The inventors also found that genetic and pharmacological interventions to deplete ACBP/DBI efficiently improves cardiac dysfunction associated with experimental HFpEF, a condition associated with aging, hypertension and obesity. Accordingly, the present disclosure relates to methods for the treatment of cardiac dysfunction comprising neutralization of ACBP/DBI.
The present invention concerns a novel in vitro assay for determining the invasive ability of brain tumour cells, in particular brain tumour stem cells. This new assay, called 3D invasion assay, is based on the analysis and comparison of the area of neurospheres grown in vitro into a Matrigel extracellular-like matrix. The invention also concerns the use of said assay for diagnosing metastatic brain tumour in subjects, for determining its prognosis, as well as for the monitoring, for the stratification, for identifying subjects at risk of metastasis, and/or predicting the metastasis-associated risk in subjects diagnosed with brain tumour.
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
UNIVERSITÉ PARIS CITÉ (France)
INSTITUT GUSTAVE ROUSSY (France)
PARIS SCIENCES ET LETTRES (France)
FONDATION IMAGINE – INSTITUT DES MALADIES GENETIQUES (France)
ASSISTANCE PUBLIQUE-HÔPITAUX DE PARIS (APHP) (France)
Inventor
Rodriguez, Raphaël
Muller, Sebastian
Cañeque, Tatiana
Colombeau, Ludovic
Thoidingjam, Leishemba Khuman
Côté, Francine
Abstract
The present invention relates to serotonin derivatives of general formula (I), and their use in the pharmaceutical field, in particular for preventing or treating metalloptosis associated disorders. The invention also relates to new serotonin derivatives of general formula (I) and their use for preventing or treating iron- and/or copper-associated disorders.
INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (France)
UNIVERSITE PARIS CITE (France)
UNIVERSITE PARIS‐SACLAY (France)
ASSISTANCE PUBLIQUE ‐ HOPITAUX DE PARIS (APHP) (France)
INSTITUT GUSTAVE ROUSSY (France)
Inventor
Turhan, Ali
Beannaceur Griscelli, Annelise
Griscelli, Franck
Jinwook, Hwang
Abstract
Cardiovascular diseases represent the leading cause of mortality and accounts for approximately one-third of deaths globally each year. During the last decade, tremendous efforts have been made to take advantage of advances in regenerative cardiology using the approaches of adult or pluripotent stem cells. However, the current protocols do not recapitulate cardiac-related architectures. Thus, there remains a need in the art for further methods for producing cardiac organoids actually mimicking a cardiac tissue, starting from pluripotent stem cells. Notably, there remains a need in the art for producing cardiac organoids comprising cardiac muscle cells and endothelial cells, including both atrium-like and ventricular-like chambers. Such cardiac organoids that reliably mimic a cardiac tissue would notably allow testing for the physiological effects of known drug substances as well as candidate molecules, particularly in embodiments wherein the said cardiac organoids are produced by starting from cells originating from patients affected with a cardiac disease or disorder such as a cardiac disease or disorder of genetic origin. It is now provided a novel matrix-free and feeder-free method of generating mammal iPSC-derived cardiac organoids, which method includes both steps of dynamic culture conditions and static culture conditions. As it is experimentally shown, cardiac organoids obtained with the matrix-free and feeder-free method disclosed herein are relevant models for testing potentially active substances on cardiac organoids obtained from iPSCs derived from subjects affected with a cardiac disease or disorder.
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
UNIVERSITÉ DE LORRAINE (France)
INSTITUT GUSTAVE ROUSSY (France)
UNIVERSITÉ PARIS-SACLAY (France)
Inventor
Mc Murtry, Stefan
El Mazria, Omar
Mir, Luis
Andre, Franck
Abstract
The present invention relates to a microcapsule that is made of bioavailable polymer, is loaded with at least one active substance and comprises at least one micrometric opening. The invention also relates to a method for obtaining said capsule and to said capsule for use in the treatment of a pathology, in particular cancer or myopathy.
The inventors herein show that purinergic receptors regulate the conversion of macrophage pro-inflammatory reprogramming into anti-inflammatory phenotype in patients suffering from COVID-19 disease. Moreover, they show that P2Y receptor agonists repress NLRP3 inflammasome-dependent IL-1b secretion, but also impair the replication and the cytopathogenic effects of SARS-CoV-2. These results therefore suggest that some purinergic receptors agonists can treat acute lung injury and respiratory disease that are associated with SARS-CoV-2 infection. In addition, their results show that antagonists of the purinergic receptors P2X impair the replication of said virus. The present invention therefore proposes to use purinergic receptors modulators and NLR3-P2Y2R immune checkpoint modulators to treat patients suffering from a virus-induced acute respiratory distress syndrome.
A61K 31/7048 - Compounds having saccharide radicals and heterocyclic rings having oxygen as a ring hetero atom, e.g. leucoglucosan, hesperidin, erythromycin, nystatin
A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
A61P 11/00 - Drugs for disorders of the respiratory system
A61K 31/196 - Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
A61K 31/64 - Sulfonylureas, e.g. glibenclamide, tolbutamide, chlorpropamide
A61K 31/191 - Acyclic acids having two or more hydroxy groups, e.g. gluconic acid
47.
A BIOMARKER AND COMPOSITIONS TO INCREASE THE THERAPEUTIC INDEX OF NEOADJUVANT IMMUNOTHERAPY IN MUSCLE-INVASIVE UROTHELIAL CARCINOMA
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITE PARIS-SACLAY (France)
Inventor
Goubet, Anne-Gaëlle
Zitvogel, Laurence
Loriot, Yohann
Abstract
The present invention relates to the treatment of locally advanced and metastatic muscle-invasive bladder cancers (MIBC). The present invention provides compositions to be used in immunotherapy of MIBC, especially in combination with an anti-PD-1/PD-L1/PD-L2 antibody-based therapy. The present invention also provides biomarkers of response to anti-PD- 1/PD-L1/PD-L2 immune checkpoint blocking antibodies (ICBs), alone or together with anti-CTLA4 antibodies and/or chemotherapy, for best guiding their neoadjuvant use and avoid unefficient administration of potentially toxic drugs to patients with localized bladder cancers.
C07K 16/28 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
A61K 39/40 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum bacterial
48.
Microbiota composition, as a marker of responsiveness to anti-PD1/PD-L1/PD-L2 antibodies and use of microbial modulators for improving the efficacy of an anti-PD1/PD-L1/PD-L2 AB-based treatment
A61K 35/744 - Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
A61K 39/00 - Medicinal preparations containing antigens or antibodies
A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum
C12Q 1/6886 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
C12Q 1/689 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for detection or identification of organisms for bacteria
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
Inventor
Allouch, Awatef
Deutsch, Eric
Perfettini, Jean-Luc
Lux, François
Tillement, Olivier
Abstract
The present disclosure relates to the field of nanomedicine, in particular for treating cancers. The present disclosure more specifically provides new methods of treating undesirable M2-polarized macrophages and/or inducing M1 macrophage polarization in a subject in need thereof, comprising administering to said subject a therapeutically effective amount of nanoparticles containing metallic elements.
A61K 49/18 - Nuclear magnetic resonance [NMR] contrast preparationsMagnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes
A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
50.
METHOD FOR IDENTIFYING COMPOUNDS USEFUL FOR THE TREATMENT OF CANCER
INSERM (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE) (France)
INSTITUT GUSTAVE ROUSSY (France)
Inventor
Brenner, Catherine
Modjtahedi, Nazanine
Abstract
The invention relates to a method for identifying compounds useful for the treatment of cancer based on assessing the ability of the compound to modulate the interaction between the AIF protein and the CHCHD4 protein.
C07K 14/47 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from animalsPeptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from humans from vertebrates from mammals
51.
Compounds with tubulin polymerisation inhibitory activity and immunomodulatory properties
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNES) (France)
INSTITUT GUSTAVE ROUSSY (France)
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM) (France)
Inventor
Alami, Mouad
Provot, Olivier
Hamze, Abdallah
Khelifi, Ilhem
Naret, Timothée
Apcher, Sébastien
Darrigrand, Romain
Abstract
The present invention relates to the Compound of following formula (I):
or a pharmaceutically acceptable salt thereof.
The present invention also relates to a pharmaceutical composition containing such a compound and a method for preparing such a compound.
C07D 401/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
C07D 403/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
52.
METHOD FOR PROCESSING AT LEAST A PRE-CONTRAST IMAGE AND A CONTRAST IMAGE RESPECTIVELY DEPICTING A BODY PART PRIOR TO AND AFTER AN INJECTION OF A FIRST DOSE OF CONTRAST AGENT
The present invention relates to method for medical imaging, the method being characterized in that it comprises the implementation, by a data processor (11b) of a second server (1b), of steps of: (a) Obtaining at least one candidate pre-contrast image and a candidate contrast image respectively depicting a body part prior to and after an injection of a first dose of contrast agent, wherein said first dose is higher than a predetermined low dose, the predetermined reduced dose being lower than a predetermined standard dose; a convolutional neural network, CNN, being trained to reconstruct, from at least a pre-contrast input image and a low dose contrast input image respectively depicting a body part prior to and after an injection of said low dose of contrast agent, a standard dose contrast image depicting said body part after an injection of said standard dose of contrast agent; (b) Simulating an injection of a second dose of contrast agent which is higher than the standard dose, wherein said simulating comprises generating a synthetic contrast image by applying the CNN to the at least one candidate pre-contrast image and the candidate contrast image.
A61B 6/00 - Apparatus or devices for radiation diagnosisApparatus or devices for radiation diagnosis combined with radiation therapy equipment
G06V 10/774 - Generating sets of training patternsBootstrap methods, e.g. bagging or boosting
G06V 10/82 - Arrangements for image or video recognition or understanding using pattern recognition or machine learning using neural networks
G16H 30/20 - ICT specially adapted for the handling or processing of medical images for handling medical images, e.g. DICOM, HL7 or PACS
G16H 30/40 - ICT specially adapted for the handling or processing of medical images for processing medical images, e.g. editing
G16H 50/20 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
G16H 50/50 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for simulation or modelling of medical disorders
G16H 50/70 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for mining of medical data, e.g. analysing previous cases of other patients
G01R 33/56 - Image enhancement or correction, e.g. subtraction or averaging techniques
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE - CNRS - (France)
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
INSTITUT GUSTAVE ROUSSY (France)
VETAGRO-SUP INSTITUT D'ENSEIGNEMENT SUPÉRIEUR ET DE RECHERCHE (France)
Inventor
Natuzzi, Marco
Brichart, Thomas
Rossetti, Fabien
Martini, Matteo
Lux, François
Tillement, Olivier
Perfettini, Jean-Luc
Louzier, Vanessa
Bonnet-Garin, Jeanne-Marie
Ayoub, Jean-Yves
Abstract
The present invention relates to the field of medical devices, more particularly the field of devices for extracting circulating molecules from the blood of a mammal, and their therapeutic uses, in particular in treating sepsis, cytokine release syndrome and/or any other form of systemic inflammatory response or cytokine shock, caused by bacterial, parasitic, fungal or viral infections, in particular caused by a viral infection, for example coronaviruses with human respiratory tract tropism.
The present invention relates to a method of predicting assessing or monitoring the sensitivity of a subject having a cancer to an immunotherapy, preferably to an immunotherapy combining at least two immunotherapeutic agents, and to corresponding kits and uses thereof. The method of predicting, assessing or monitoring the sensitivity of a subject having a tumor to an immunotherapy typically comprises a step of assessing, before any immunotherapeutic treatment step in the subject, the presence of CD4+CD25highCD39high T cells in a tumor sample of the subject, the presence of CD4+CD25highCD39high T cells in the tumor sample of the subject being indicative of sensitivity of the subject to the immunotherapy, and the absence of CD4+CD25highCD39high T cells in the tumor sample of the subject being indicative of resistance of the subject to the immunotherapy.
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
INSTITUT GUSTAVE ROUSSY (France)
Inventor
Taoufik, Yassine
De Goër De Herve, Marie-Ghislaine Madeleine
Abstract
The present invention relates to a new and specific T-cell therapy strategy based on the use of memory stem T-cells (Tscm), in particular highly functional memory stem T-cells (Tscm) negatively selected on the basis of inhibitory receptor expression. This new cellular immunotherapy may be applied to PML patients but also to other infections or cancers for which the specific memory T cell responses are functionally impaired.
INSERM (Institut National de la Santé et de la Recherche Médicale) (France)
Ceinge Biotecnologie Avanzate SCARL (Italy)
Institut Gustave Roussy (France)
Sorbonne Université (France)
Université Paris Cité (France)
Assistance Publique-Hôpitaux de Paris (APHP) (France)
Inventor
Maiuri, Chiara
Kroemer, Guido
Pol, Jonathan
Salvatore, Francesco
De Palma, Fatima
Del Monaco, Valentina
Abstract
The present invention relates to methods and compositions for the care of breast cancer, from diagnosis to treatment management. The inventors show that LINC01087 downregulation contributes to a more aggressive phenotype of BC, and could represents a novel and promising specific biomarker for the diagnosis of triple-negative breast cancer. The inventors show that LINC01087 upregulation contributes to a less aggressive phenotype of BC, and could represents a novel and promising specific biomarker for the diagnosis of luminal BCs. The invention relates to a method comprising the steps of: i) determining the expression level of the long intergenic non-coding RNA 01087 (LINC01087) in a sample obtained from the subject, and ii) comparing the expression level determined at step i) with a predetermined reference value, wherein detecting difference between the expression level determined at step i) and the predetermined reference value is indicative of an aggressive TNBC or less aggressive luminal BCs.
C12Q 1/6886 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
57.
NOVEL SEROTONIN DERIVATIVES AND THEIR USES FOR TREATING IRON-ASSOCIATED DISORDERS
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (France)
INSTITUT GUSTAVE ROUSSY (France)
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
INSTITUT CURIE (France)
UNIVERSITÉ PARIS CITÉ (France)
Inventor
Rodriguez, Raphaël
Cote, Francine
Coman, Tereza
Debieu, Sylvain
Caneque Cobo, Tatiana
Hermine, Olivier
Muller, Sebastian
Falabrègue, Marion
Abstract
The present invention relates to novel serotonin derivatives of formula (I) or a pharmaceutically acceptable salt and/or solvate thereof. Another object of the present invention relates to the use of compound of formula (I) as a drug, in particular in the prevention and/or the treatment of iron overload-associated disorders.
A freeze-dried powder for preparing a thermogel including: from 1% to 35% of 2-[(3-aminopropyl)amino]ethanethiol or one of its pharmaceutically acceptable salt; from 40% to 85% of one or more poloxamer; and from 0.1% to 20% of one or more carbohydrate compound.
A61K 31/145 - Amines, e.g. amantadine having sulfur atoms, e.g. thiurams (N—C(S)—S—C(S)—N or N—C(S)—S—S—C(S)—N)Sulfinylamines (—N=SO)Sulfonylamines (—N=SO2)
A61K 9/19 - Particulate form, e.g. powders lyophilised
A61K 47/34 - Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
A61K 47/26 - Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharidesDerivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
Inventor
Fidelle, Marine
Zitvogel, Laurence
Daillere, Romain
Rauber Conrad
Abstract
The present invention relates to the field of anticancer immunotherapy. In particular, the present invention concerns the role of the MAdCAM-1/α4β7 axis the gut microbiota in the efficacy of cancer treatments and provides methods for determining if a patient is likely to benefit from a cancer treatment, more precisely, and imuno-oncology (l-O) therapy, such as a treatment comprising administration of an antibody directed against immune checkpoint blockers PD1, PD-L1 or PD-L2 alone or together with CTLA4 and/or chemotherapy. The present invention also provides methods to improve the efficacy of such a treatment in patients in need thereof.
G01N 33/569 - ImmunoassayBiospecific binding assayMaterials therefor for microorganisms, e.g. protozoa, bacteria, viruses
G01N 33/574 - ImmunoassayBiospecific binding assayMaterials therefor for cancer
G01N 33/68 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving proteins, peptides or amino acids
60.
Microbial compositions for improving the efficacy of anticancer treatments based on immune checkpoint inhibitors and/or tyrosine kinase inhibitors and markers of responsiveness to such treatments
The invention pertains to the use of bacteria selected amongst Alistipes senegalensis, Dorea longicatena and Eubacterium siraeum for inducing immunostimulation in a patient in combination with an anti-cancer immunotherapy with an immune checkpoint inhibitor (ICI) and/or a tyrosine kinase inhibitor (TKI). The invention also relates to methods for assessing the probability that a patient respond to a treatment with an ICI and/or a TKI, based on measuring the relative abundances of immunotolerant bacterial species (Clostridium hathewayi, Clostridium clostridioforme and Clostridium boltae) and/or immunostimulatory bacterial species (Akkermansia muciniphila, Bacteroides salyersiae, Alistipes senegalensis, Dorea longicatena and Eubacterium siraeum) in the patient's gut microbiota.
FUNDAÇÃO D. ANNA DE SOMMER CHAMPALIMAUD (Portugal)
UNIVERSITE PARIS-SACLAY (France)
TRANSGENE (France)
Inventor
Zitvogel, Laurence
Fahrner, Jean-Eudes
Maeurer, Markus
De Sousa, Eric
Lerias, Joana
Abstract
The application pertains to biomarkers for assessing whether an individual is likely to resist to an infection by a SARS-CoV-2 virus or is susceptible to SARS-CoV-2.
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (France)
INSTITUT GUSTAVE ROUSSY (France)
Inventor
Brenner, Catherine
Taran, Frédéric
Cintrat, Jean-Christophe
Perfettini, Jean-Luc
Abstract
The invention relates to compounds capable of inducing autophagy and metabolic reprogramming and to the use thereof as cardioprotectors, in particular in the context of anti-cancer therapy.
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
FONDATION IMAGINE (France)
INSTITUT GUSTAVE ROUSSY (France)
UNIVERSITÉ PARIS CITE (France)
UNIVERSITÉ PARIS-SACLAY (France)
UNIVERSITÉ TOULOUSE III – PAUL SABATIER (France)
ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE TOULOUSE (France)
Inventor
Causse Brunet, Erika
Mercher, Thomas
Babin, Loélia
Robert, Elie
Darchen, Alice
Lamant, Laurence
Meggetto-Pradelle, Fabienne
Abstract
Anaplastic large cell lymphoma (ALCL) is a rare and aggressive peripheral T-cell lymphoma affects lymph nodes and extra-nodal sites with characteristic skin lesions. Approximatively half of the tumors express the NPM1-ALK fusion from the translocation t(2;5)(p23;q32). In the present study, the inventors identify ROR2 as progressively up regulated thought tumorigenesis. Patient samples show a significantly high ROR2 expression (transcriptomic data) as well as a strong ROR2 protein expression (IHC) with some tumors displaying a clear membrane signal. ROR2 mRNA expression level is also positively correlated to NPM-ALK expression level in tumor cells and is not expressed in normal T cells. In addition, ROR2 protein level is significantly increased in resistant cells to the ALK inhibitor, crizotinib, used in clinical trials for children with refractory tumors. This result opens the road to ROR2 specific therapies: ROR2 inhibitors, monoclonal antibodies therapies or even ROR2 specific CAR cells, including for ALCL ALK(+) resistant tumors.
C07K 16/28 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
A61K 47/68 - Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additivesTargeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
A61K 39/00 - Medicinal preparations containing antigens or antibodies
A61P 35/02 - Antineoplastic agents specific for leukemia
A61K 31/4545 - Non-condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum
64.
METHOD FOR TRAINING A DECISION SYSTEM FOR SEGMENTING MEDICAL IMAGES
The invention relates to a method implemented by computer means for training a decision system for segmenting medical images (6) from a training set of annotated medical images, said segments belonging to at least one class, each annotation (LB) of said medical images including quantitative information about a number of pixels of the image (6) that belongs to each of said classes, said method using weakly-supervised algorithm based on a percentage of the pixels of said image belonging to a concerned class.
Identification of effective targets alleviating the programmed cell removal (PrCR) of tumor cells by macrophages is of very high interest. The present inventors have identified that the cyclin-dependent kinase inhibitor p21 protein is a strong regulator of the macrophage-mediated PrCR. Also, they showed that the adoptive transfer of p21 overexpressing monocytes induces macrophage PrCR and transition from an anti-inflammatory to a pro-inflammatory phenotype in vivo, delays cancer progression and increases significantly the overall survival of mice engrafted with cancer cells. The present invention therefore concerns therapeutic compositions comprising monocytes that over-express the cyclin-dependent kinase inhibitor p21 protein, and their use for treating mammals suffering from cancer, especially leukemia.
A61K 38/17 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from animalsPeptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from humans
C12N 15/90 - Stable introduction of foreign DNA into chromosome
A61K 35/15 - Cells of the myeloid line, e.g. granulocytes, basophils, eosinophils, neutrophils, leucocytes, monocytes, macrophages or mast cellsMyeloid precursor cellsAntigen-presenting cells, e.g. dendritic cells
A61P 35/02 - Antineoplastic agents specific for leukemia
A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
66.
BIOLOGICAL MARKER OF INTESTINAL DYSBIOSIS, USEFUL FOR PREDICTING THE RESPONSE OF A CANCER PATIENT TO AN ANTI-PD1 DRUG
The present invention relates to the field of anticancer treatment. In particular, the present invention concerns the role of the gut microbiota in the efficacy of immune checkpoints inhibitors (ICI)-based treatments and provides methods for determining if a patient is likely to benefit from an ICI-based treatment, more precisely, treatment comprising administration of an antibody directed against PD1 or PD-L1. The present invention provides a method for stratifying cancer patients according to their potential need of bacterial complementation before receiving an ICI-based treatment. The present invention also provides a simple method for determining whether an individual has an intestinal dysbiosis.
The present invention provides tools for stratifying patients suffering from osteosarcoma, in order to identify patients having poor prognosis tumors. The invention also pertains to the use of an inhibitor of the PPARγ pathway as an antineoplastic treatment to improve the overall survival of patients with a poor prognosis osteosarcoma.
The present invention concerns a novel in vitro assay for determining the invasive ability of brain tumour cells, in particular brain tumour stem cells. This new assay, called 3D invasion assay, is based on the analysis and comparison of the area of neurospheres grown in vitro into a Matrigel extracellular-like matrix. The invention also concerns the use of said assay for diagnosing metastatic brain tumour in subjects, for determining its prognosis, as well as for the monitoring, for the stratification, for identifying subjects at risk of metastasis, and/or predicting the metastasis-associated risk in subjects diagnosed with brain tumour.
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
UNIVERSITE PARIS-SACLAY (France)
Inventor
Zitvogel, Laurence
Iebba, Valerio
Abstract
The present invention relates to a method for in vitro determining if an individual having a renal cell cancer (RCC) is likely to respond to a treatment with an anti-PD1/PD-L1/PD-L2 Ab-based therapy, based on the analysis of the microbiota present in a stool sample from said individual. Twelve models useful to perform the above method are disclosed, as well as tools designed to easily perform this method.
C12Q 1/6886 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
C12Q 1/689 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for detection or identification of organisms for bacteria
G06F 17/18 - Complex mathematical operations for evaluating statistical data
70.
Madrasin-derivative compounds, composition and uses thereof for treating cancer
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT GUSTAVE ROUSSY (France)
UNIVERSITE PARIS-SACLAY (France)
Inventor
Apcher, Sébastien
Alami, Mouad
Darrigrand, Romain
Messaoudi, Samir
Salgues, Valérie
Renko, Zafiarisoa Dolor
Yen-Pon, Expedite
Abstract
The present invention relates to the fields of medicine and in particular cancer treatment. The invention more specifically relates to new compounds which are typically for use as a medicament. In particular, the invention relates to the use of these new compounds for increasing the presentation, typically the production and presentation, of Pioneer Translation Products (PTPs)-derived antigens by cells, in particular cancer cells, or changing the immunopeptidome, in a subject, and inducing or stimulating an immune response in the subject. The present disclosure also relates to uses of such compounds, in particular to prepare a pharmaceutical composition and/or to allow or improve the efficiency of a therapy in a subject in need thereof. The invention also discloses methods for treating a disease, in particular cancer, for preventing or treating cancer metastasis and/or cancer recurrence, in a subject. The present invention in addition provides kits suitable for preparing a composition according to the present invention and/or for implementing the herein described methods.
A61K 31/517 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
A61K 31/5377 - 1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
A61K 31/661 - Phosphorus acids or esters thereof not having P—C bonds, e.g. fosfosal, dichlorvos, malathion
A61K 31/7064 - Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
Institut National de la Sante et de la Recherche Medicale (INSERM) (France)
Assistance Publique - Hopitaux de Paris (France)
Universite de Versailles - St Quentin en Yvelines (France)
Inventor
Vainchenker, William
Ugo, Valerie
James, Chloe
Le Couedic, Jean-Pierre
Casadevall, Nicole
Abstract
The present invention concerns the V617F variant of the protein-tyrosine kinase JAK2, said variant being responsible for Vaquez Polyglobulia. The invention also relates to a first intention diagnostic method for erythrocytosis and thrombocytosis allowing their association with myeloproliferative disorders, or to the detection of the JAK2 V617F variant in myeloproliferative disorders allowing their reclassification in a new nosological group.
G01N 33/574 - ImmunoassayBiospecific binding assayMaterials therefor for cancer
C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
The present invention relates to the combined use of a neuropilin-1 (Nrp-1) neutralizing agent and of a programmed cell death-1 (PD-1) neutralizing agent for killing cancer cells, typically for treating cancer, as well as to corresponding pharmaceutical compositions and kits, and to corresponding diagnostic and therapeutic methods. The invention further relates to in vitro, ex vivo and in vivo methods for detecting CD8+ TILs capable of recognizing cancer cells, for predicting the response of a subject to anti-PD-1 treatment of cancer, and for identifying a subject who responds therapeutically to a treatment of cancer with an antibody combination therapy comprising anti-Nrp-1 and anti-PD-1 antibodies.
A61K 35/17 - LymphocytesB-cellsT-cellsNatural killer cellsInterferon-activated or cytokine-activated lymphocytes
C07K 16/28 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
Board of Regents, The University of Texas System (USA)
Institut Gustave Roussy (France)
Inventor
Wargo, Jennifer A.
Gopalakrishnan, Vancheswaran
Andrews, Miles C.
Zitvogel, Laurence
Iebba, Valerio
Abstract
Described herein are methods and compositions for treating cancer and for predicting a subjects' response to combination checkpoint inhibitor therapy. Aspects of the disclosure relate to a method of treating cancer and/or reducing toxicity to a therapy in a subject comprising administering to the subject a composition comprising at least one isolated or purified population of bacteria belonging to one or more of the genera Flavonifractor, Dielma, Akkermansia, Alistipes, Bacteroides, Butyricimonas, Vampirovibrio, Tyzzerella, Parabacteroides distasonis, Fournierella, Fournierella massiliensis, Eisenbergiella tayi, Tissierellales, Hungateiclostridium thermocellum, Dorea formicigenerans, Caloramator coolhaasi, Muricomes, Geosporobacter, Prevotella paludivivens, Lactobacillus secaliphilus, Bacteroides fmegoldii, Lactobacillus johnsonii, Parapedobacter composti, and Anaerotignum lactatifermentans and wherein the method further comprises treating the subject with a combination of (i) a PD-1, PDL1, or PDL2 inhibitor and (ii) a CTLA-4, B7-1, or B7-2 inhibitor.
C12Q 1/689 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for detection or identification of organisms for bacteria
74.
METHODS FOR DETECTING AND TREATING COVID PATIENTS REQUIRING INTENSIVE CARE
The present invention provides novel, easy-to-monitor and sensitive parameters, biomarkers and methods for the prediction of SARS-CoV-2 patients outcome, allowing in particular an early identification of patients evolving towards severe COVID-19 forms. The examples presented in the application show that a calprotectin-driven emergency myelopoisis in patients undergoing a switch toward a severe form of COVID 19 generates an innate immune cell signature of severe COVID-19. More precisely, the present inventors have found that the amount of CD14low/CD16+ monocytes, of HLA-DRlowclassical monocytes and of CD16lowneutrophils can independently or concomitantly be used as biomarkers of the severity of betacoronavirus infection, before the switch to the severe form of the infection (and related painful symptoms) actually occurs. The methods of the invention comprise the quantification, in a biological sample from an infected subject, of the amount of these immune cells. In addition, the Inventors have observed a surprising burst of calprotectin levels in COVID-19 patients that are undergoing a switch toward a severe disease. They therefore propose to use calprotectin plasma level as a biomarker of COVID-19 switch to severe form, and also as a therapeutic target for alleviating the disease symptoms.
C07K 14/47 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from animalsPeptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from humans from vertebrates from mammals
C07K 14/74 - Major histocompatibility complex [MHC]
C12N 5/0787 - Granulocytes, e.g. basophils, eosinophils, neutrophils or mast cells
The inventors herein show that purinergic receptors regulate the conversion of macrophage pro-inflammatory reprogramming into anti-inflammatory phenotype in patients suffering from COVID-19 disease. Moreover, they show that P2Y receptor agonists repress NLRP3 inflammasome-dependent IL-1b secretion, but also impair the replication and the cytopathogenic effects of SARS-CoV-2. These results therefore suggest that some purinergic receptors agonists can treat acute lung injury and respiratory disease that are associated with SARS-CoV-2 infection. In addition, their results show that antagonists of the purinergic receptors P2X impair the replication of said virus. The present invention therefore proposes to use purinergic receptors modulators and NLR3-P2Y2R immune checkpoint modulators to treat patients suffering from a virus-induced acute respiratory distress syndrome.
A61K 31/7084 - Compounds having two nucleosides or nucleotides, e.g. nicotinamide-adenine dinucleotide, flavine-adenine dinucleotide
A61K 31/675 - Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
A61K 31/7072 - Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine
A61P 11/00 - Drugs for disorders of the respiratory system
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE - CNRS - (France)
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
INSTITUT GUSTAVE ROUSSY (France)
VETAGRO-SUP INSTITUT D'ENSEIGNEMENT SUPÉRIEUR ET DE RECHERCHE (France)
Inventor
Natuzzi, Marco
Brichart, Thomas
Rossetti, Fabien
Martini, Matteo
Lux, François
Tillement, Olivier
Perfettini, Jean-Luc
Louzier, Vanessa
Bonnet-Garin, Jeanne-Marie
Ayoub, Jean-Yves
Abstract
The present invention relates to the field of medical devices, more particularly the field of devices for extracting circulating molecules from the blood of a mammal, and to the therapeutic uses thereof, in particular in the treatment of sepsis, of cytokine release syndrome and/or of any other form of systemic inflammatory response or cytokine storm, caused by bacterial, parasitic, fungal or viral infections, in particular caused by a viral infection, for example coronaviruses with human respiratory tract tropism.
A61M 1/16 - Dialysis systemsArtificial kidneysBlood oxygenators with membranes
A61M 1/34 - Filtering material out of the blood by passing it through a membrane, i.e. hemofiltration, diafiltration
A61M 1/36 - Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation
77.
Microbiota composition, as a marker of responsiveness to anti-PD1/PD-L1/PD-L2 antibodies and use of microbial modulators for improving the efficacy of an anti-PD1/PD-L1/PD-L2 ab-based
A61K 35/744 - Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum
C12Q 1/6886 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
C12Q 1/689 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for detection or identification of organisms for bacteria
A61K 39/00 - Medicinal preparations containing antigens or antibodies
78.
METHOD FOR IDENTIFYING COMPOUNDS USEFUL FOR THE TREATMENT OF CANCER
INSERM(INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE) (France)
INSTITUT GUSTAVE ROUSSY (France)
Inventor
Brenner, Catherine
Modjtahedi, Nazanine
Abstract
The invention relates to a method for identifying compounds useful for the treatment of cancer, based on assessing the ability of the compound to modulate the interaction between the AIF protein and the CHCHD4 protein.
G01N 33/547 - Synthetic resin with antigen or antibody attached to the carrier via a bridging agent
G01N 33/68 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving proteins, peptides or amino acids
G01N 33/574 - ImmunoassayBiospecific binding assayMaterials therefor for cancer
C07K 14/47 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from animalsPeptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from humans from vertebrates from mammals
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
CEINGE BIOTECNOLOGIE AVANZATE SCARL (Italy)
INSTITUT GUSTAVE ROUSSY (France)
SORBONNE UNIVERSITÉ (France)
UNIVERSITÉ DE PARIS (France)
ASSISTANCE PUBLIQUE-HÔPITAUX DE PARIS (APHP) (France)
Inventor
Maiuri, Chiara
Kroemer, Guido
Pol, Jonathan
Salvatore, Francesco
De Palma, Fatima
Del Monaco, Valentina
Abstract
The present invention relates to methods and compositions for the care of breast cancer, from diagnosis to treatment management. The inventors show that LINC01087 downregulation contributes to a more aggressive phenotype of BC, and could represents a novel and promising specific biomarker for the diagnosis of triple-negative breast cancer. The inventors show that LINC01087 upregulation contributes to a less aggressive phenotype of BC, and could represents a novel and promising specific biomarker for the diagnosis of luminal BCs. The invention relates to a method comprising the steps of: i) determining the expression level of the long intergenic non-coding RNA 01087 (LINC01087) in a sample obtained from the subject, and ii) comparing the expression level determined at step i) with a predetermined reference value, wherein detecting difference between the expression level determined at step i) and the predetermined reference value is indicative of an aggressive TNBC or less aggressive luminal BCs.
C12Q 1/6886 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
80.
Means for transporting persons with reduced mobility comprising a device with for connecting to aserum holder, associated connecting assembly
A system for transporting persons with reduced mobility includes a chassis having two lateral cross members, a device for connecting to an IV pole including a rod and a wheeled support attached to an end of the rod, the connection device including an attachment support fixed to the chassis, a coupling element designed to be solidly fixed to the rod, a member for connecting the coupling element to the attachment support, a lateral stop attached to at least one of the cross members, the lateral stop being built and arranged to brace the wheeled support in relation to the chassis and to position the IV pole laterally in relation to the transportation system.
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (France)
INSTITUT GUSTAVE-ROUSSY (France)
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM) (France)
Inventor
Alami, Mouad
Provot, Olivier
Hamze, Abdallah
Khelifi, Ilhem
Naret, Timothée
Apcher, Sébastien
Darrigrand, Romain
Abstract
The present invention relates to the Compound of following formula (I):
or a pharmaceutically acceptable salt thereof.
The present invention also relates to a pharmaceutical composition containing such a compound and a method for preparing such a compound.
C07D 401/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
C07D 403/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
A freeze-dried powder for preparing a thermogel comprising: - from 1% to 35% of 2-[(3-aminopropyl)amino]ethanethiol or one of its pharmaceutically acceptable salt; - from 40% to 85% of one or more poloxamer; and - from 0,1% to 20% of one or more carbohydrate compound.
A61K 31/145 - Amines, e.g. amantadine having sulfur atoms, e.g. thiurams (N—C(S)—S—C(S)—N or N—C(S)—S—S—C(S)—N)Sulfinylamines (—N=SO)Sulfonylamines (—N=SO2)
A61K 47/26 - Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharidesDerivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
A61K 47/34 - Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
A61P 17/16 - Emollients or protectives, e.g. against radiation
A61K 9/00 - Medicinal preparations characterised by special physical form
Centre National de La Recherche Scientifique - CNRS - (France)
INSERM (Institut National de la Sante et de la Recherche Médicale) (France)
Institut Gustave Roussy (France)
Inventor
Lux, François
Tillement, Olivier
Perfettini, Jean-Luc
Deutsch, Eric
Law, Frédéric
Allouch, Awatef
Abstract
The invention relates to methods for treating tumors. In particular, the invention provides novel use of nanoparticles in combination with ionizing radiations for treating tumors, wherein the combined effect of nanoparticles induces senescence and/or cannibalism of the tumor cells.
Centre National de la Recherche Scientifique (France)
Université Paris-Saclay (France)
Inventor
Deschamps, Frédéric
De Baere, Thierry
Tselikas, Lambros
Isoardo, Thomas
Huang, Nicolas
Moine, Laurence
Tsapis, Nicolas
Fattal, Elias
Abstract
The present invention relates to a water-in-oil emulsion comprising a continuous oil phase and an aqueous phase dispersed in the form of drops, the said aqueous phase comprising polyester-based nanoparticles and at least one therapeutic agent.
A61K 31/4745 - QuinolinesIsoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenanthrolines
A61K 31/555 - Heterocyclic compounds containing heavy metals, e.g. hemin, hematin, melarsoprol
A61K 31/704 - Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin, digitoxin
A61K 47/44 - Oils, fats or waxes according to two or more groups of Natural or modified natural oils, fats or waxes, e.g. castor oil, polyethoxylated castor oil, montan wax, lignite, shellac, rosin, beeswax or lanolin
B82Y 5/00 - Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
85.
Antibody which is Directed Against Galectin-9 and is an Inhibitor of the Suppressor Activity of Regulatory T Lymphocytes
Centre National de la Recherche Scientifique (France)
Institut Gustave Roussy (France)
Cellvax (France)
Universite Paris Saclay (France)
Inventor
Delhem, Nadira
Busson, Pierre
Morales, Olivier
Barjon, Clement
Mrizak, Dhafer
Lhuillier, Claire
Mustapha, Rami
Abstract
The disclosure relates to an antibody which is directed against galectin-9 and is an inhibitor of the suppressor activity of regulatory T lymphocytes, and also to the use of this antibody for the treatment of diseases associated with the suppressor activity of regulatory T lymphocytes, in particular the treatment of cancer.
C07K 16/28 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
C07K 16/30 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
C07K 16/18 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans
A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum
A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
86.
NOVEL THERAPEUTIC COMBINATIONS COMPRISING DERIVATIVES OF OXAZAPHOSPHORINES FOR THE TREATMENT OF CANCER
The present invention relates to novel therapeutic combinations comprising an oxazaphosphorine derivative and an immune checkpoint modulator for the treatment or the prevention of cancers.
A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum
C07K 16/28 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
87.
MICROBIAL COMPOSITIONS FOR IMPROVING THE EFFICACY OF ANTICANCER TREATMENTS BASED ON IMMUNE CHECKPOINT INHIBITORS AND/OR TYROSINE KINASE INHIBITORS AND MARKERS OF RESPONSIVENESS TO SUCH TREATMENTS
The invention pertains to the use of bacteria selected amongst Alistipes senegalensis, Dorea longicatena and Eubacterium siraeum for inducing immunostimulation in a patient in combination with an anti-cancer immunotherapy with an immune checkpoint inhibitor (ICI) and/or a tyrosine kinase inhibitor (TKI). The invention also relates to methods for assessing the probability that a patient respond to a treatment with an ICI and/or a TKI, based on measuring the relative abundances of immunotolerant bacterial species (Clostridium hathewayi, Clostridium clostridioforme and Clostridium boltae) and/or immunostimulatory bacterial species (Akkermansia muciniphila, Bacteroides salyersiae, Alistipes senegalensis, Dorea longicatena and Eubacterium siraeum) in the patient's gut microbiota.
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE - CNRS - (France)
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITE PARIS-SACLAY (France)
Inventor
Allouch, Awatef
Deutsch, Eric
Perfettini, Jean-Luc
Lux, François
Tillement, Olivier
Abstract
The present disclosure relates to the field of nanomedicine, in particular for treating cancers. The present disclosure more specifically provides new methods of treating undesirable M2-polarized macrophages and/or inducing M1 macrophage polarization in a subject in need thereof, comprising administering to said subject a therapeutically effective amount of nanoparticles containing metallic elements.
A61K 41/00 - Medicinal preparations obtained by treating materials with wave energy or particle radiation
A61K 47/69 - Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additivesTargeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
A61K 49/18 - Nuclear magnetic resonance [NMR] contrast preparationsMagnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes
A61P 1/16 - Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
A61P 9/10 - Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
A61P 11/00 - Drugs for disorders of the respiratory system
The present inventors have demonstrated that it is possible to control the secretory profile and phagocytosis function of pro-inflammatory macrophages, notably after irradiation on injured sites, by silencing the expression of a tumor suppressor gene called DUOX1 (dual oxidase 1). They therefore propose to inhibit the expression of the DUOX1 gene or the activity of the DUOX1 enzyme in tumor-associated macrophages for inducing a strong anti-tumor effect. They also propose to combine this treatment with a radiotherapy treatment, as said treatment is potentiated when DUOX1 is inhibited.
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM) (France)
COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (France)
UNIVERSITE PARIS-SACLAY (France)
Inventor
Perfettini, Jean Luc
Deutsch, Eric
Brenner, Catherine
Cintrat, Jean-Christophe
Taran, Frederic
Abstract
The present invention is drawn to the use of Minaprine dihydrochloride and analogs thereof, for reducing tumor growth when administered to a patient suffering from cancer.
in vivoin vivo, delays cancer progression and increases significantly the overall survival of mice engrafted with cancer cells. The present invention therefore concerns therapeutic compositions comprising monocytes that over-express the cyclin-dependent kinase inhibitor p21 protein, and their use for treating mammals suffering from cancer, especially leukemia.
A61K 35/15 - Cells of the myeloid line, e.g. granulocytes, basophils, eosinophils, neutrophils, leucocytes, monocytes, macrophages or mast cellsMyeloid precursor cellsAntigen-presenting cells, e.g. dendritic cells
The present invention proposes a radiomics-based biomarker for detecting the presence and the density of tumor infiltrating CD8 T-cells in a solid tumor without having to use any biopsy of said tumor. The invention also proposes to use this information to assess the immune phenotype of said solid tumor. In a particular embodiment, the invention proposes to prognose the survival and/or the treatment efficiency of cancer patients treated with immunotherapy such as anti-PD-1/PD-L1 monotherapy.
G16H 30/40 - ICT specially adapted for the handling or processing of medical images for processing medical images, e.g. editing
G16H 50/20 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
93.
COMBINATION OF ONCOLYTIC VIRUS WITH IMMUNE CHECKPOINT MODULATORS
The present invention provides a combination comprising at least an oncolytic virus and one or more immune checkpoint modulator(s) for use for the treatment of a proliferative disease such as cancer. It also relates to a kit comprising said oncolytic virus and said one or more immune checkpoint modulator(s) in separate containers. It also concerns a pharmaceutical composition comprising effective amount of said oncolytic virus and said one or more immune checkpoint modulator(s).
A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum
C07K 16/28 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
C12N 5/00 - Undifferentiated human, animal or plant cells, e.g. cell linesTissuesCultivation or maintenance thereofCulture media therefor
C12N 7/00 - Viruses, e.g. bacteriophagesCompositions thereofPreparation or purification thereof
94.
Microbiota composition, as a marker of responsiveness to chemotherapy, and use of microbial modulators (pre-, pro- or synbiotics) for improving the efficacy of a cancer treatment
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
INSTITUT NATIONAL DE RECHERCHE POUR L'AGRICULTURE, L'ALIMENTATION ET L'ENVIRONNEMENT (France)
Inventor
Zitvogel, Laurence
Gomperts Boneca, Ivo
Lepage, Patricia
Viaud, Sophie
Daillere, Romain
Abstract
The present invention provides methods for determining if a patient is likely to benefit from a cancer treatment, by determining if said patient has a gut dysbiosis with an over representation of certain bacterial species. The present invention also provides probiotic strains to improve the efficacy of a cancer treatment, especially chemotherapy, in patients in need thereof.
The invention relates to the prognosis and treatment of colon cancer. In particular, the present invention concerns the role of intestinal microbiota in the anticancer immune response elicited by ileal enterocytes succumbing to apoptosis, and provides immunogenic compositions for treating colorectal cancer (CRC), as well as signatures for prognosing CRC evolution.
The present inventors identified for the first time a germline genomic alteration that accounts for familial myeloproliferative neoplasms (MPN) and myeloid malignancies. More precisely, they identified a 700 kb germline duplication that proposes patients to essential thrombocythemia (ET) with a high frequency of evolution to myelofibrosis (MF), secondary myelodysplastic syndromes (MDS) or acute myeloid leukemia (AML). Two out of the 6 duplicated genes (namely ATG2B and GSKIP) have been shown to be overexpressed in hematopoietic progenitors, and this overexpression cooperates with classical mutations in JAK2, MPL, and CALR to generate the MPN phenotype. The presence of the 700 kb germline duplication is thus of poor prognosis for a MPN patient. The present invention discloses a method for detecting a predisposition of developing a MPN, as well as a prognostic method for assessing the probability that an ET-suffering patient will develop a myelofibrosis, a secondary MDS or an AML. It also discloses a treating method for delaying MPN worsening, said treating method involving the inhibition of the ATG2B and GSKIP duplicated genes.
C12Q 1/6886 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
G01N 33/574 - ImmunoassayBiospecific binding assayMaterials therefor for cancer
A pharmaceutical liquid suspension comprising: temozolomide or a salt thereof; at least one agent controlling the solid state of temozolomide in suspension; a pharmaceutically acceptable liquid vehicle; and optionally at least one acid in a quantity so that the pH of the composition is below 5; or a powder blend for reconstituting said suspension, is provided.
A61K 31/495 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two nitrogen atoms as the only ring hetero atoms, e.g. piperazine
Although tumor-associated macrophages have been extensively studied in the control of response to radiotherapy, the molecular mechanisms involved in the ionizing radiation-mediated activation of macrophages remain elusive. Here the present inventors show that ionizing radiation induces the expression of interferon-regulatory factor 5 (IRF5) promoting thus macrophage activation toward a pro-inflammatory phenotype. They reveal that the activation of the Ataxia telangiectasia mutated (ATM) kinase is required for ionizing radiation-elicited macrophage activation, but also for macrophage reprogramming after treatments with γ-interferon, lipopolysaccharide or chemotherapeutic agent (such as cis-platin), underscoring the fact that the kinase ATM plays a central role during macrophage phenotypic switching toward a proinflammatory phenotype. They further demonstrate that NADPH oxidase 2 (NOX2)-dependent ROS production is upstream to ATM activation and is essential during this process. They also report that hypoxic conditions and the inhibition of any component of this signaling pathway (NOX2, ROS and ATM) impairs pro-inflammatory activation of macrophages and predicts a poor tumor response to preoperative radiotherapy in locally advanced rectal cancer. Altogether, these results identify a novel signaling pathway involved in macrophage activation that may enhance effectiveness of radiotherapy through the re-programming of tumor infiltrating macrophages.
C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
C12Q 1/6886 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
IMAGINE INSTITUT DES MALADIES GENETIQUES NECKER ENFANTS MALADES (France)
UNIVERSITE PARIS DESCARTES (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
Inventor
Coman, Tereza
Cote, Francine
Hermine, Olivier
Fouquet, Guillemette
Rossignol, Julien
Abstract
The invention relates to the combined use of selective serotonin reuptake inhibitors (SSRIs) and hematopoietic growth factors as a drug and particularly for treating cytopenia related to hematopoietic diseases or chemotherapy, and also to a pharmaceutical kit comprising both SSRIs and hematopoietic growth factors. This combination is more particularly used for treating patients presenting cytopenia, and patients in need of chemotherapy and more particularly to reduce length of chemotherapy-induced aplasia.
A61K 31/343 - Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
A61K 31/4525 - Non-condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
100.
ANTI-NEUROPILIN-1 AND ANTI-PROGRAMMED CELL DEATH-1 COMBINATION THERAPY FOR TREATING CANCER
The present invention relates to the combined use of a neuropilin-1 (Nrp-1) neutralizing agent and of a programmed cell death-1 (PD-1) neutralizing agent for killing cancer cells, typically for treating cancer, as well as to corresponding pharmaceutical compositions and kits, and to corresponding diagnostic and therapeutic methods. The invention further relates to in vitro, ex vivo and in vivo methods for detecting CD8+ TILs capable of recognizing cancer cells, for predicting the response of a subject to anti-PD-1 treatment of cancer, and for identifying a subject who respond therapeutically to a treatment of cancer with an antibody combination therapy comprising anti-Nrp-1 and anti-PD-1 antibodies.
C07K 16/28 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum
A61K 35/17 - LymphocytesB-cellsT-cellsNatural killer cellsInterferon-activated or cytokine-activated lymphocytes