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BioWorld - Monday, August 3, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

Sep. 29, 2017

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FDA awards orphan drug designation to Cascadian's tucatinib

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AzurRx reports initial data from ongoing phase IIa trial of MS-1819-SD

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Synergys Biotherapeutics receives grant to support SYN-001 development

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Diamyd to design first clinical trial of Remygen

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NIDA grant supports Camino Pharma's development of compounds for substance use disorders

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New lung cancer study to utilize Inivata's InVision liquid biopsy platform

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Safety explored in first-in-human study of KHK-4083, a monoclonal antibody targeting OX40

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Eidos Therapeutics doses first cohort in AG-10 phase I study

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Topline results from phase I/II study of SciFluor's SF-0166 for DME

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Inhaled sodium cromoglycate formulation PA-101 reduces cough in IPF patients

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Villin-1 as a biomarker of intestinal ischemia reperfusion injury

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Achaogen awarded contract for development of C-Scape

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Protagenic Therapeutics' PT-00114 shows efficacy in animal models

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GlaxoSmithKline divulges CD73 inhibitors

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FDA gives Emergency Use Authorization to Chembio for DPP Zika system test

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Merck & Co. patents novel monobactam derivatives for bacterial infections

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Raze Therapeutics identifies 3-PGDH inhibitors

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Global Alliance for TB Drug Development patents compounds for tuberculosis

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New York University discloses Wnt signaling inhibitors

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FDA grants orphan drug designation to rimeporide for Duchenne muscular dystrophy

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SI-613 begins phase II trial in Japan for enthesopathy

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FDA approves Verzenio in breast cancer

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Japanese orphan drug designation for olaparib for BRCA-positive breast cancer

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First subject enrolled in phase III study of TRC-101 in chronic kidney disease

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Quidel announces progress in acquisition of Alere's BNP business

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FDA grants priority review to Amitiza sNDA for pediatric functional constipation

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TLR3 identified as novel target for preventing cardiac ischemia reperfusion injury

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Phase Ib data do not support progression of PRX-003 for psoriasis

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U.S. contract supports progression of InBios point-of-care diagnostic test for B. anthracis

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Zynerba reports promising data from phase II trial of ZYN-002 for fragile X syndrome

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Curemark completes enrollment in phase III trial of CM-AT in autism

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FDA grants priority review to Linhaliq NDA

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FDA priority review for Perjeta sBLA for adjuvant treatment of HER2-positive early breast cancer

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NIAID grant supports development of thermostable trivalent Ebola vaccine

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