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BioWorld - Monday, January 26, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

Aug. 4, 2017

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Mitsubishi Tanabe Pharma offers overview of first quarter of fiscal 2017

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Pfizer reflects on milestones of second quarter 2017

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MiMedx initiates phase III study of AmnioFix Injectable following phase IIb results

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Pellficure Pharmaceuticals begins enrollment in phase I trial of PCUR-101 in metastatic CRPR

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Proclara Biosciences' GAIM-Ig fusion NPT-189 blocks assembly of amyloid aggregates

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Intec reports phase I results for AP-CBD/THC

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Vaccibody files German clinical trial application for cancer neoantigen vaccine VB10.NEO

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FDA approves Mavyret for HCV

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Cormedix provides update on ongoing phase III study of Neutrolin

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Novel peptide-based viral inactivator shows promise as treatment against ZIKV in vivo

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EMA announces business continuity plan to prepare for U.K.'s withdrawal from the E.U.

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Sentinel Oncology receives Innovate UK grant to study SOL-784

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Bristol-Myers Squibb to acquire IFM Therapeutics

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FDA advisory committee recommends approval of Xeljanz for psoriatic arthritis

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ANGPTL3 antagonism is associated with reduced risk of atherosclerotic cardiovascular disease

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Takeda and Molecular Templates establish new oncology drug discovery collaboration

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Novel susceptibility variants for Alzheimer's disease identified in Chinese subjects

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Realm Therapeutics submits IND for PR-013 for allergic conjunctivitis

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EpiVax receives funding to support development of personalized cancer vaccines

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Oxeia acquires rights to SUN-11031 from KineMed

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FDA approves Vyxeos for two types of AML

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U.S. researchers patent antiparasitic compounds

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Beth Israel Deaconess Medical Center discloses CRAC blockers

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Janssen Pharmaceutica identifies MAP3K14 inhibitors

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Sichuan Haisco Pharmaceutical divulges new antivirals

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NIH researchers develop mouse model to track Zika virus transmission

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Dolutegravir superior in combination with NRTIs for treating HIV-1 infection

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FDA awards orphan drug designation to Applied Genetic Technologies' gene therapy candidate for XLRP

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Portola resubmits AndexXa BLA

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Dynavax updates status of Heplisav-B submission following FDA advisory committee meeting

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