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BioWorld - Friday, December 5, 2025
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BioWorld Science
Dec. 24, 2018
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miRNA551b found as therapeutic target for AML
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ITI-333 shows promise for the treatment of pain and substance abuse-derived disorders
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Scripps Research Institute presents mu-opioid receptor ligand SR-17018
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CSIC Zika virus vaccine shows promise in mouse infection models
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Ionis begins phase I/II study of ION-TTR-LRx in healthy subjects and patients with hATTR
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New tumor organoid includes microenvironment
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Responses seen with blinatumomab monotherapy in relapsed/refractory B-cell non-Hodgkin's lymphoma
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Rivaroxaban thromboprophylaxis effective only during treatment period in cancer patients
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Quinazoline can serve as a novel core structure in the design of potent BRD4 inhibitors
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ASLAN Pharmaceuticals presents phase II data for ASLAN-003 in AML patients
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Geranylgeranyl diphosphate synthase inhibitors RAM-2061, RAM-2093 show promise for multiple myeloma
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Aimmune Therapeutics submits IND application for AR-201 as treatment of egg allergy
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Combination approach revs up beta cell production
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Platform could prove broad strategy against emerging viruses
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MUC17 and PCNX1 as novel biomarkers of chemotherapy response in breast cancer
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Elzonris receives FDA approval for the treatment of blastic plasmacytoid dendritic cell neoplasm
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Novartis receives approval in the E.U. for expanded indication for Kisqali
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Suglat Tablets approved for additional indication of type 1 diabetes mellitus in Japan
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FDA approves Inbrija
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FDA grants early approval for Ultomiris for the treatment of adults with PNH
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Merck KGaA and Pfizer terminate JAVELIN Ovarian 100 study of avelumab
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Phase II TRAXAR study does not meet primary endpoint
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Life Science Institute initiates exploratory clinical trial of CL-2020 in epidermolysis bullosa
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Novartis reports compounds for treatment of parasitic diseases
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Esteve Pharmaceuticals patent reports agents for the treatment of pain
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Hemlibra subcutaneous injection approved in Japan for hemophilia A without inhibitors
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Chugai receives approval in Japan for Tecentriq for additional dosing in NSCLC
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FDA approves IND for anti-GM-CSF monoclonal antibody TJM2
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