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BioWorld - Thursday, December 11, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Aug. 22, 2016

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H3 Biomedicine initiates phase I study of H3B-8800 in MDS, AML and CMML

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FDA grants clearance for Alere i RSV rapid molecular test

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FDA approves Pfizer's Troxyca ER

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Celgene Quanticel Research describes novel JARID1A/1B inhibitor at ACS

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ABCB6 is a genetic modifier of the severity of hereditary porphyria

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AB Science patents atitumoral agents

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Bayer Pharma discloses sGC activators

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F12 and STC2 genes as independent prognostic factors in breast cancer

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EMA accepts Portola Pharmaceuticals' MAA for Indexxa

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FDA extends iGlarLixi NDA review following submission of additional information

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Cancer Research Technology develops ENPP2 inhibitors

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Chinese scientists present Nav1.7 channel blockers

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Phase II results demonstrate clinical activity for venetoclax monotherapy in patients with AML

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Rio Grande Neurosciences terminates binding letter agreement with Endonovo Therapeutics

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PATH initiates phase I trial of MCV-5 meningococcal conjugate vaccine

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Randox Biochip Array Technology allows rapid determination of ApoE4 status in plasma

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Shionogi initiates phase III trial of S-649266 to treat carbapenem-resistant Gram-negative bacteria

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Vaccinex's VX-15 gets FDA orphan drug designation for the treatment of Huntington's disease

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PZM-21 is a potent, novel mu-opioid receptor agonist with reduced side effects

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New phase II trial explores safety and immunogenicity of TSI-GSD-210 for Western equine encephalitis

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FDA grants tentative approval to Supernus Pharmaceuticals' NDA for Trokendi

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FDA accepts IND for Zymeworks' ZW-25

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Nordic Nanovector announces completion of several arms in betalutin trial

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Arca Biopharma randomizes 100th patient in GENETIC-AF clinical trial

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Nutrinia and Morristown close deal to fund oral insulin trials

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