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BioWorld - Wednesday, March 11, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

Jan. 8, 2016

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Mice homozygous for LGMD2I-causing FKRP mutation show progressive myopathy

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Genetic association meta-analysis identifies 10 novel risk loci for atopic dermatitis

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X-Chem and MD Anderson partner to discover and develop novel cancer therapies

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Merck & Co. forms partnership with BH4 pathway modulator developer Quartet Medicine

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AGTC and BCM Families Foundation collaborate on AAV-based gene therapy for blue cone monochromacy

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BioAtla and Sinobioway select first programs under CAB collaboration in China

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EMA will review Trevyent under centralized authorization procedure

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U.S. Army starts phase I trial of dengue challenge virus

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OBI Pharma's immunotherapy OBI-833 enters first-in-human trial

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First patient treated in I trial of SBP-101 for pancreatic cancer

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Faron Pharmaceuticals reports topline results from phase II study of Traumakine

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Clearside Biomedical reports topline data from phase II study of CLS-TA

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Ionis Pharmaceuticals' IONIS-HTT Rx receives FDA orphan drug designation

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First-in-class Dub inhibitor shows preclinical antitumor activity

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Millendo licenses phase II polycystic ovary syndrome candidate from AstraZeneca

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Universite Pierre et Marie Curie discloses DNA gyrase inhibitors

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Katholieke Universiteit Leuven and UCB present PI4KIII inhibitors

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State University of New Jersey reports antibacterial compounds

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New U.K. study investigates tocilizumab for PAH

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SYK inhibitor shows acceptable safety profile in patients with DLBCL and FL

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Paratek expects results from phase III trial of omadacycline in ABSSSI in mid-2016

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FDA grants fast track designation to Bendavia for primary mitochondrial myopathy

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Novo Nordisk seeks European approval for nonacog beta pegol for hemophilia B

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Anacor submits NDA for crisaborole for atopic dermatitis

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FDA accepts for review sarilumab BLA for rheumatoid arthritis

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FDA grants orphan drug and breakthrough therapy designations to setmelanotide

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FDA clears IND application for pediatric trial of TB-403

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FDA grants priority review for sNDA for Viekira Pak in genotype 1b HCV and cirrhosis

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