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BioWorld - Friday, April 3, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

Dec. 7, 2017

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FDA awards orphan drug status to SPR-001 for congenital adrenal hyperplasia

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National Cancer Center Japan testing DS-8201 in uterine carcinosarcoma

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Clementia initiates phase III study of palovarotene for fibrodysplasia ossificans progressive

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Novel ex vivo cell and gene therapy regenerates entire human epidermis in patient with JEB

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Low-dose LMTM monotherapy may improve Alzheimer's disease impairments

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Positive data reported from immunotherapy combination study of DPX-Survivac

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Pimozide stabilizes neuromuscular junction transmission in patients with ALS

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ChemomAb raises funds to support development of lead product

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Janssen Biotech exercises option to collaborate with Idorsia on aprocitentan

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Nexus BioPharma licenses rights to KV-001 for rapid reduction of adipose tissue

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ObsEva begins proof-of-concept trial of OBE-022

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Phase III data show efficacy of LMWF-5A in severe knee osteoarthritis

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TAK-935/OV-935 obtains orphan drug status in U.S. for Dravet syndrome

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First patient dosed in Novan's phase Ib study of SB-414 in atopic dermatitis

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New phase I/II trial to study abexinostat with ibrutinib in relapsed or refractory DLBCL or MCL

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Galectin Therapeutics reports positive results from phase IIb study of GR-MD-02

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FDA approves Novo Nordisk's Ozempic for type 2 diabetes

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National University of Singapore and Academia Sinica patent dual JAK-2/HDAC6 inhibitors

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Novel anti-TSHR chimeric antigen receptors identified at the University of Florida

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Exicure presents novel antisense oligonucleotides targeteing IL-17RA

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Phase II study of MGL-3196 in NASH meets primary endpoint

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Shire enters agreement with Rani Therapeutics to study Rani Pill technology

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FDA grants orphan drug designation to STP-705 for cholangiocarcinoma

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FDA grants full approval to Avastin for recurrent glioblastoma in adults

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FDA grants priority review for rucaparib sNDA for maintenance therapy in ovarian cancer

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Novartis commences tender offer for Advanced Accelerator Applications

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VE-303 begins first-in-human study, awarded U.S. orphan drug designation

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New phase I trial studies DNX-2401 in pediatric diffuse intrinsic pontine glioma

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