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BioWorld - Wednesday, December 10, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Feb. 29, 2016

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VCE-004.8 shows promise for the treatment of scleroderma

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Facio receives funding from the Dutch FSHD Foundation

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Esteve and UAB expand gene therapy platform with therapies for Sanfilippo B and Hunter's syndromes

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Baxalta seeks FDA approvals for Adynovate for use in pediatric patients and surgical settings

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PharmaMar starts phase II trial of microtubule inhibitor PM-184 in breast cancer

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Heat Biologics updates progress of phase II trial of HS-410 for non-muscle invasive bladder cancer

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Hydra Biosciences patents TrpC5 antagonists

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Nuevolution discloses RORgamma modulators

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Eolas Therapeutics develops orexin receptor modulators

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Changzhou Runnor Biological Technology describes EGFR mutant inhibitors

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Bristol-Myers Squibb initiates phase I/IIa study of BMS-986205 with nivolumab in advanced cancers

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Ortho-McNeil-Janssen Pharmaceuticals divulges GluN2B receptor inhibitors

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Encouraging phase I data for Biota's RSV fusion inhibitor BTA-585

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Gilead's Descovy receives positive CHMP opinion for HIV infection

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Aurora Biopharma secures grant for trials of CAR T-cell therapy for glioblastoma and osteosarcoma

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EMA CHMP issues positive opinion for ixekizumab for plaque psoriasis

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Daiichi Sankyo initiates phase I trial of U3-1784 for solid tumors

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Takeda's ixazomib receives orphan drug designation in Japan for multiple myeloma

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FDA approves Afinitor for progressive, nonfunctional GI and lung neuroendocrine tumors

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EMA committee recommends E.U. approval of Alprolix to treat hemophilia B

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Rare Disease Day: SONIA trials to clarify the potential of nitisinone in treating alkaptonuria

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EMA's CHMP recommends approval of Opdivo for two new indications

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Intravaginal prasterone shows promise for female sexual dysfunction

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CHMP recommends approval of Taiho's Lonsurf for metastatic colorectal cancer

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Genentech's lebrikizumab achieves primary endpoint in one of two phase III trials in severe asthma

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EMA committee hands down positive opinion for Viekirax + Exviera label expansion

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FDA approves Gazyva for use in follicular lymphoma

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