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BioWorld - Monday, January 26, 2026
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BioWorld Science
Aug. 4, 2017
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Mitsubishi Tanabe Pharma offers overview of first quarter of fiscal 2017
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Pfizer reflects on milestones of second quarter 2017
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MiMedx initiates phase III study of AmnioFix Injectable following phase IIb results
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Pellficure Pharmaceuticals begins enrollment in phase I trial of PCUR-101 in metastatic CRPR
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Proclara Biosciences' GAIM-Ig fusion NPT-189 blocks assembly of amyloid aggregates
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Intec reports phase I results for AP-CBD/THC
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Vaccibody files German clinical trial application for cancer neoantigen vaccine VB10.NEO
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FDA approves Mavyret for HCV
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Cormedix provides update on ongoing phase III study of Neutrolin
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Novel peptide-based viral inactivator shows promise as treatment against ZIKV in vivo
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EMA announces business continuity plan to prepare for U.K.'s withdrawal from the E.U.
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Sentinel Oncology receives Innovate UK grant to study SOL-784
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Bristol-Myers Squibb to acquire IFM Therapeutics
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FDA advisory committee recommends approval of Xeljanz for psoriatic arthritis
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ANGPTL3 antagonism is associated with reduced risk of atherosclerotic cardiovascular disease
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Takeda and Molecular Templates establish new oncology drug discovery collaboration
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Novel susceptibility variants for Alzheimer's disease identified in Chinese subjects
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Realm Therapeutics submits IND for PR-013 for allergic conjunctivitis
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EpiVax receives funding to support development of personalized cancer vaccines
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Oxeia acquires rights to SUN-11031 from KineMed
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FDA approves Vyxeos for two types of AML
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U.S. researchers patent antiparasitic compounds
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Beth Israel Deaconess Medical Center discloses CRAC blockers
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Janssen Pharmaceutica identifies MAP3K14 inhibitors
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Sichuan Haisco Pharmaceutical divulges new antivirals
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NIH researchers develop mouse model to track Zika virus transmission
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Dolutegravir superior in combination with NRTIs for treating HIV-1 infection
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FDA awards orphan drug designation to Applied Genetic Technologies' gene therapy candidate for XLRP
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Portola resubmits AndexXa BLA
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Dynavax updates status of Heplisav-B submission following FDA advisory committee meeting
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