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BioWorld - Friday, December 5, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

March 27, 2018

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Vertex studies VX-659 triple combination in phase III cystic fibrosis study

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Nektar initiates phase I/II study of NKTR-262 alone and in combination for solid tumor malignancies

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AbbVie opens phase I trial of ABBV-744 in advanced prostate cancer and AML

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Male contraceptive 11beta-MNTDC reduces testosterone in healthy male volunteers

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Phase III efficacy and safety data reported for vibegron in overactive bladder

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Phase III trials of rimegepant in migraine meet coprimary endpoints

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Allecra reports phase II data on cefepime/AAI-101 in cUTI

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Protagonist stops phase IIb study of PTG-100 for ulcerative colitis based on futility analysis

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FDA grants breakthrough therapy designation to enfortumab vedotin

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Loxo completes rolling NDA for larotrectinib in U.S.

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Amag submits NDA for bremelanotide for hypoactive sexual desire disorder

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EMA grants PRIME designation for lumasiran in primary hyperoxaluria type 1

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Acorda submits MAA to EMA for Inbrija

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EMA committee recommends approval of new dosing schedules for Opdivo in E.U.

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Celgene tests new purine-based compound with antimalarial properties

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FORMA Therapeutics establishes collaboration with Arpeggio Biosciences

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Sanofi seeks U.S. and E.U. approval for sotagliflozin in type 1 diabetes

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Vitaros end-of-review meeting scheduled by FDA

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Japanese approval for Orkedia

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Hemlibra approved in Japan

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Hernicore approved in Japan to treat lumbar disc herniation

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Bayer Pharma divluges new adenosine receptor A2B antagonists

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Nippon Kayaku obtains Japanese approval for trastuzumab biosimilar

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Jiangsu Hengrui Medicine Co., Shanghai Hengrui Pharmaceutical Co. patent factor XIa inhibitors

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AdPueriVitam discovers novel NMDA receptor antagonists

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Velcade approved in Japan for primary macroglobulinemia and lymphoplasmacytic lymphoma

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Gilead identifies novel Toll-like receptor 8 modulators

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RaQualia receives milestone payment from EA Pharma

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New Toll-like receptor 7/8 agonists patented by GlaxoSmithKline

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ACT-539313 safe and well tolerated in first-in-human study

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