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BioWorld - Tuesday, December 23, 2025
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BioWorld Science
March 1, 2017
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ATYR-1940 granted U.S. orphan drug designation for the treatment of limb girdle muscular dystrophy
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FDA grants orphan drug designation to ustekinumab for the treatment of pediatric ulcerative colitis
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EMA committee hands down positive opinion for 8-week regimen of Viekirax + Exviera
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FDA requests additional information to complete IND review for Titan's ropinirole implant
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FDA awards fast track designation to Immunopulse IL-12 for metastatic melanoma
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WHO publishes list of antibiotic-resistant priority pathogens
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Sanofi seeks Japanese approval for dupilumab for atopic dermatitis
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FDA grants rare pediatric disease designation to SB-318 for MPS I
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Phase III pediatric study of Latuda for bipolar I depression meets primary endpoint
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Immune Pharmaceuticals broadens enrollment criteria in bullous pemphigoid study of bertilimumab
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Accera announces results from phase III study of AC-1204 for mild to moderate Alzheimer's disease
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Bremelanotide improves desire and distress in hypoactive sexual desire disorder
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miR-223 found to play a role in alcoholic liver disease
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Astellas and Affinivax enter worldwide partnership for MAPS vaccine targeting pneumococcus
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Vycellix and Moffitt Cancer Center establish collaborative research agreement
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TGFB2 has a pathogenic role in Alzheimer's disease and dementia with Lewy bodies
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Cancer Research UK and HitGen announce license agreement in lung cancer
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Kevzara becomes available in Canada
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Immunologic responses seen with vesigenurtucel-L in non-muscle invasive bladder cancer
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FDA grants priority review to avelumab BLA for metastatic urothelial carcinoma
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Johnson & Johnson completes acquisition of Abbott Medical Optics
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Perrigo signs agreement to divest Tysabri royalty stream
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FDA approves Xermelo for carcinoid syndrome diarrhea
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ZUMA-1 study of axicabtagene ciloleucel meets primary endpoint of objective response rate
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FDA accepts Dynavax's response to Heplisav-B complete response letter
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