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BioWorld - Wednesday, December 24, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Jan. 9, 2014

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A functional serotonin receptor polymorphism as a biomarker for cardiovascular disease

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GlycoMimetics presents data from phase II trial of GMI-1070 in sickle cell disease

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Stress-related transcription factor promotes fibrosis and oncogenesis

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Application of site-directed RNA editing to correct disease-causing genetic mutations

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Development of a novel ROR1 peptide-based cancer vaccine

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Astellas Pharma and ClearPath Development to build vaccine company portfolio

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Emmaus Medical completes all patient visits in phase III sickle cell disease trial

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Trovagene and US Oncology Research collaborate on urine-based KRAS testing study

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ERYtech plans phase II study of ERY-ASP in pancreatic cancer

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DURECT grants Impax worldwide rights to develop and commercialize ELADUR pain patch

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Amunix and Janssen extend worldwide collaboration and licensing agreement

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Galena enrolls first patient in phase II trial of GALE-301 cancer immunotherapy in ovarian cancer

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Immunovative Therapies updates Allovax plans

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Takeda's vedolizumab enters phase III trials in Japan for ulcerative colitis and Crohn's disease

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Adocia initiates phase IIa trial of ultra-fast acting formulation of insulin lispro

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FDA accepts NPS Pharmaceuticals' BLA for Natpara for hypoparathyroidism

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Reata reports discovery of epoxidized triterpenoids

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Austrian group patents novel agents for protozoal infections

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Ribomic presents new aptamers for rheumatoid arthritis and other disorders

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Novel LPA-1 receptor antagonists presented by Roche

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Roche divulges novel FABP inhibitors

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FDA approves phase IIb study of PRO-140 for HIV-1

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TeaRx begins phase II trial of novel anticoagulant in Russia

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Catalyst Pharmaceutical reports cardiac safety results from phase III Firdapse trial

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Forest Laboratories enters definitive agreement to acquire Aptalis

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Bristol-Myers Squibb and AstraZeneca gain FDA approval for Forxiga in type 2 diabetes

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Daiichi Sankyo files applications for oral, once-daily anticoagulant edoxaban in Europe and U.S.

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GSK obtains accelerated FDA approval for use of Mekinist in combination with Tafinlar

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