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BioWorld - Friday, December 5, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Feb. 1, 2018

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Armis Biopharma's Ximycin designated as QIDP by FDA

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Sumitomo Dainippon Pharma highlights progress of third quarter of fiscal 2017

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First patient treated in phase III study of BeiGene's tislelizumab

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Dermira begins phase IIb study of lebrikizumab in moderate to severe atopic dermatitis

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Preclinical data presented for adipoRon in cholangiocarcinoma

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Sage Therapeutics' SAGE-217 improves sleep efficiency and sleep time in model of insomnia

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FDA gives Protalix Biotherapeutics' PRX-102 fast track designation

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Oncolix sponsoring evaluation of Prolanta for other gynecological cancers

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Cara Therapeutics begins pivotal phase III study of Korsuva in CKD-associated pruritus

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Acasti initiates TRILOGY trials of CaPre in patients with severe hypertriglyceridemia

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Vertex selects VX-659 and VX-445 to advance into phase III cystic fibrosis triple combination trials

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Phase III U.S. study of transdermal patch for schizophrenia meets primary endpoint

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IDO1 as an indicator of poor outcome in anal squamous cell carcinoma

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First patient treated in clinical study of ONC-201 in children with H3 K27M mutant glioma

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AbGenomics' neihulizumab granted orphan drug status in U.S. for aGvHD

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Vaxart's oral influenza tablet vaccine demonstrates reduction in rate of influenza infection

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Medshine Discovery patents new PPAR agonists

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Gemphire initiates phase IIa trial of gemcabene for pediatric NAFLD

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Seattle Genetics enters definitive merger agreement to acquire Cascadian Therapeutics

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Cadila Healthcare divulges novel RORgamma inverse agonists

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Bristol-Myers Squibb discloses PD-1/PD-L1 interaction inhibitors

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Japanese researchers present compounds for Parkinson's disease

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Galecto Biotech discovers galectin inhibitors

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AstraZeneca initiates phase IIa study of AZD-9567 in rheumatoid arthritis

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Lanreotide effective for prolonged control of carcinoid syndrome symptoms

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