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BioWorld - Thursday, December 25, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Feb. 9, 2018

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FDA accepts SIGA Technologies' NDA for TPOXX

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Daiichi Sankyo studies DS-1205c with osimertinib for metastatic or unresectable EGFR-mutant NSCLC

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New phase II umbrella trial studies novel agents for the management of relapsed ovarian cancer

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V ClinBio acquires 49.98% equity stake in Cellix Bio

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Rebinyn launched in the U.S.for the treatment of hemophilia B

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Sanofi files tender offer for Bioverativ

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Columbia University divulges novel CKI-epsilon inhibitors

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Q Biomed receives exclusive option for glaucoma biomarker GDF-15

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FDA priority review granted for antimalarial tafenoquine

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New RET kinase inhibitors identified at Blueprint Medicines

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Roche discovers new serine protease HTRA1 inhibitors

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Shanghai Yingli Pharmaceutical presents new TGF-beta receptor type-1 inhibitors

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Novel ACKR3 antagonists patented by Idorsia Pharmaceuticals

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Therapix Biosciences clarifies regulatory pathway for THX-110

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ABAC Therapeutics identifies novel antibacterials

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AstraZeneca announces pipeline highlights of fourth quarter 2017

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SPK-8011 shown safe and effective for hemophilia A

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GlaxoSmithKline reviews milestones of fourth quarter 2017

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Implantable device allows photodynamic therapy for tumors deep in the body

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Vifor prepares to begin phase I trial of oral ferroportin inhibitor VIT-2763

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Significant reductions in LDL-cholesterol seen with MGL-3196 in phase II tiral

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uniQure presents further clinical data on AMT-060 for hemophilia B

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Rexahn Pharmaceuticals to collaborate with Zhejiang Haichang Biotechnology on RX-0201

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Lonza Pharma & Biotech and Denali Therapeutics partner on biologics

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Bristol-Myers Squibb offers overview of fourth quarter 2017

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FDA grants orphan drug designation to Xeris' ready-to-use, liquid-stable glucagon

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Phase III trials of peficitinib in rheumatoid arthritis meet primary endpoints

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Fujifilm and Takeda establish regenerative medicine collaboration to treat heart failure

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Treatment begins in phase II SHINE-1 study of scar reduction with EB-001

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FDA approves Zytiga with prednisone for metastatic high-risk castration-sensitive prostate cancer

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