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BioWorld - Thursday, March 28, 2024
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BioWorld Science
Aug. 1, 2017
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GSK reflects on accomplishments of second quarter 2017
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Takeda presents key events of first quarter of fiscal 2017
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Exposure to MeNZB vaccine associated with reduced rates of gonorrhea diagnosis
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First-in-human results for personalized RNA mutanome vaccine IVAC MUTANOME
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FDA grants priority review to RBP-6000 NDA, clearance for buprenorphine assay
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Kite Pharma submits MAA to EMA for axicabtagene ciloleucel
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PellePharm announces topline phase II data for topical patidegib in Gorlin syndrome
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Syndros, the first and only FDA-approved liquid dronabinol, becomes available by prescription
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BLU-667, a RET inhibitor, shows promise for RET-driven thyroid cancer
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Antigen Express and Merck & Co. agree to test AE-37 with Keytruda in triple-negative breast cancer
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BLA submission for trastuzumab biosimilar ABP-980
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Isogenica licenses antibody libraries to Takeda
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FDA grants orphan drug designation to RA-101495 for PNH
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Bayer discloses soluble guanylate cyclase activators
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Aerie collaborates with DSM on technology to deliver compounds for retinal diseases
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FDA accepts for review BLA for trastuzumab biosimilar CT-P6
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Chemerin receptor antagonists presented by Shenzhen Institute of Advanced Technology
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Celgene details pipeline developments of second quarter 2017
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Recro submits NDA for intravenous meloxicam for postoperative pain
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Phase III MAP US study of RHB-104 in Crohn's disease cleared to continue
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New tau PET ligands [18F]AM-PBB3 and [18F]PM-PBB3 evaluated in humans
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Bristol-Myers Squibb and Clovis sign clinical collaboration agreement to test Opdivo with Rubraca
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FDA clears IND for phase I study of PTI-125 for Alzheimer's disease
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Intercept reports results from trials of obeticholic acid in PSC and NASH
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Emergent BioSolutions' development of auto-injector for nerve agent antidote gets financial support
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Kitov announces NDA submission for KIT-302
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Loxo to acquire Redx's BTK inhibitor program
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FDA awards breakthrough therapy designation to acalabrutinib for mantle cell lymphoma
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Lumosa initiates phase I trial of LT-3001 for acute ischemic stroke
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Nerlynx launched in U.S.
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Astellas seeks Japanese approval for fidaxomicin for infectious enteritis caused by C. difficile
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