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BioWorld - Wednesday, December 10, 2025
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BioWorld Science
Nov. 15, 2016
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Yisheng Biopharma to collaborate with The Scripps Research Institute in developing new AIDS vaccine
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Novel benzoselenazole derivatives as PET tracers for non-invasive assessment of Abeta plaques
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S100A8/A9 is a potent serum and molecular imaging biomarker in seronegative arthritis
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Ocular Therapeutix reports positive results for phase III trial of Dextenza
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Capsazepine improves impaired lung mechanics during endotoxemia
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FDA grants orphan and fast track designations to ARMO BioSciences' AM-0010
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FDA transfers EUA for ReEBOV Ebola Antigen Rapid Test to Zalgen
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Pfizer enters CRADA with NCI to evaluate three immunotherapy agents
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EMA's CHMP recommends granting marketing authorization to Afstyla
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OpGen collaborates with Merck & Co. on rapid diagnostics to tackle antibiotic resistance
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Genfit initiates pediatric program for elafibranor in NAFLD/NASH
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Texas A&M University patents antimycobacterial agents
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Repros reports promising topline data from phase II studies of Proellex for uterine fibroids
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Katholieke Universiteit Leuven discloses PMDT nucleoside phosphonates
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FDA issues complete response letter for Heplisav-B BLA
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Xiamen University describes ALK and/or c-Met inhibitors
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Novartis develops FXR agonists
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FDA awards orphan drug designation to ECCS-50 for scleroderma
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Vallaurix presents MC1 receptor agonists
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Seizure-induced glial activation in the hippocampus suppressed by the novel NAAA inhibitor ARN-16186
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Novel delta opioid receptor agonist NC-2800 shows high anxiolytic and antidepressant activity
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ERYTECH Pharma withdraws Graspa MAA in Europe
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Reata Pharmaceuticals announces plans to study bardoxolone methyl in new indication
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Sanofi Genzyme opts in to expand rights to codevelop, co-commercialize Alnylam's fitusiran
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Pantoprazole decreases phlebotomy need in HFE-related hemochromatosis
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Acticor Biotech and Mediolanum Farmaceutici enter agreement regarding ACT-017 for stroke
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CHMP supports approval of AbbVie's Humira for adolescents with hidradenitis suppurativa
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Midostaurin NDA granted priority review by FDA
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