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BioWorld - Friday, May 8, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

April 27, 2016

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Novartis offers overview of first quarter 2016

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First-in-human results show potential of Ad26.ZEBOV and MVA-BN Filo Ebola vaccines

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Lipoic acid shown to reduce brain atrophy and exert clinical benefit in MS

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ARN-6039: a promising treatment for neuroinflammatory demyelinating disease

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Some improvements seen with calpain inhibitor ALA-1.0 in a rat model of traumatic brain injury

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eFFECTOR Therapeutics describes activity of anticancer Mnk1/2 inhibitor eFT-508

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Midatech Pharma reports preclinical pharmacokinetic data with Q-Octreotide

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AnGes and VIDO-InterVac collaborate to develop Ebola polyclonal antibody therapy

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FDA grants fast track designation for recAP in acute kidney injury

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hVIVO and SEEK in joint venture investment to develop vaccines against influenza and flu

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Positive preliminary data presented from the Tanzanite phase II trial

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Acerta Pharma patents BTK inhibitors

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Takeda Pharmaceutical announces TBK1 inhibitors

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TGF-beta receptor inhibitors described in recent Lilly patent

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Merck KGaA divulges BTK inhibtors

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First patient dosed in Exicure's phase I study of AST-005

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Prometic Life Sciences provides new data from phase II trial of PBI-4050

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Bayer Schering Pharma presents CDK inhibitors

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FDA grants breakthrough therapy designations to Ilaris for rare types of periodic fever syndromes

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Ironwood Pharmaceuticals gains exclusive U.S. rights to lesinurad

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FDA grants orphan drug designation to Fibrocell Science's FCX-013

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Zymeworks and GSK enter second bispecific antibody agreement

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FDA outlines requirements for Catalyst's planned Firdapse NDA resubmission

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Queensland Health and University of Queensland collaborate on Zika virus detection test

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Queen's University Belfast and Domainex receive award to advance NSCLC treatments

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Sun Pharma and partners establish malaria elimination demonstration project

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Ariad initiates phase I/II trial of oral AP-32788 in NSCLC

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FDA clears phase II trial of ezutromid in DMD to open in U.S.

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FDA issues complete response letter for digital medicine

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