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BioWorld - Monday, December 22, 2025
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BioWorld Science
March 2, 2018
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Convert Pharmaceuticals secures funding to advance lead cancer drug
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First infant treated in Longeveron's mesenchymal stem cell therapy trial
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Concert selects CTP-692 for development as adjuvant treatment for schizophrenia
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FDA grants breakthrough therapy designation for GC-4419 for the reduction of severe oral mucositis
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Innovimmune Biotherapeutics' INV-25 reduces tumor growth in vivo
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Heat Biologics announces positive results from phase II trial of HS-110 for NSCLC
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Patients being enrolled in phase II study of JNJ-56136379 for chronic HBV infection
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FDA fast track designation granted to Fibrogen's pamrevlumab for unresectable pancreatic cancer
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Initiation of phase II study of BMS-986263 in subjects with advanced hepatitis fibrosis
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Dong-A begins first-in-human trial of botanical drug candidate DA-9805
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Novartis presents novel SPPL2a inhibitor as a potent immunomodulator
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Patient enrollment ongoing in AstraZeneca's phase II study of AZD-8601
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Phase II study of IRL-790 is enrolling patients with Parkinson's disease dyskinesia
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TES Pharma creates first potent and selective inhibitor of human ACMSD
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Sublocade becomes available as first and only monthly injectable buprenorphine in the U.S.
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Antisense Therapeutics gains ethics approval to begin phase II trial of ATL-1102 in DMD
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Qingdao Marine Biomedical Research Institute patents new ER stress inhibitors
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Neomed Institute launches spin-out Neomed Therapeutics 1
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Shenzhen Targetrx Biotechnology divulges BTK inhibitors
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Positive results from bioequivalence study of Biohaven's rimegepant Zydis orally dissolving tablets
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Novel DGAT2 inhibitors presented by Pfizer
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FDA accepts for review Dupixent sBLA for moderate to severe asthma
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Verona announces phase IIa topline data for RPL-554 in cystic fibrosis
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French researchers present novel NMDA receptor agonists
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Merck & Co. patents new CYP8B1 inhibitors
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Reata releases data from phase II trial of omaveloxolone in patients with mitochondrial myopathies
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Acumen selects Avid Bioservices for process development, manufacturing of Alzheimer's candidate
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FDA accepts Remoxy ER NDA
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IRP1 targeting ameliorates Chuvash polycythemia in mice
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