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BioWorld - Tuesday, March 10, 2026
Home » Newsletters » BioWorld Science

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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