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BioWorld - Friday, December 5, 2025
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BioWorld Science
June 26, 2017
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Vaccibody reports results from phase I of VB C-01 study
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[203Pb]-AR-RMX completes exploratory trial in somatostatin receptor-positive neuroendocrine tumors
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Devonian to begin testing Thykamine in atopic dermatitis
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Ultragenyx reaches agreement on burosumab BLA clinical data package
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EMA gives positive opinion to Gilead Sciences' Vosevi
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FDA gives breakthrough therapy designation to CR-845 from Cara Therapeutics
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EMA's CHMP supports approval of adalimumab biosimilar Imraldi
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Preliminary phase I/II results for epacadostat plus pembrolizumab in patients with SCCHN
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Alexion Pharmaceuticals receives positive opinion from EMA to extend Soliris indication
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Eisai seeks Japanese approval for Lenvima in HCC
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EMA committee hands down positive opinion on pediatric formulation of Mimpara
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Merck & Co. discloses leukotriene BLT1 receptor antagonists
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Novel SSAO inhibitor UD-014 ameliorates experimental diabetic nephropathy
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Gan & Lee Pharmaceuticals divulges CDK4 and CDK6 inhibitors
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Naeja-Rgm Pharmaceuticals patents cephem derivatives
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EMA's CHMP grants positive opinion for tivozanib for the first-line treatment of advanced RCC
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Daiichi Sankyo develops probe to image B7-H3-expressing tumors
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U.K. MHRA approves Redx's phase Ib/IIa trial of porcupine inhibitor RXC-004
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AstraZeneca's Faslodex receives positive opinion in E.U.
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Roche identifies cannabinoid CB2 receptor agonists
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EMA supports E.U. approval of Maviret for HCV
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Hinova Pharmaceuticals discovers URAT1 inhibitors
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Takeda and Biological E partner on low-cost combination vaccines
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Merck KGaA's cladribine earns positive opinion from CHMP for relapsing forms of multiple sclerosis
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EMA committee recommends approval of Kisqali
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Signs of efficacy seen with AMG-557 in systemic lupus erythematosus trial
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FDA approves Bevyxxa for hospital and extended-duration prophylaxis of VTE
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EC approves eslicarbazepine acetate monotherapy for newly diagnosed partial-onset epilepsy
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