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BioWorld - Tuesday, December 30, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Dec. 5, 2017

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Stanford University describes novel adrenergic receptor modulators

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Saniona selects preclinical candidate for neuropathic pain and chronic itching

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Roche's idasanutlin receives U.S. orphan designation for polycythemia vera

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FDA names setmelanotide an orphan drug for treating leptin receptor deficiency

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Ra Pharmaceuticals reports interim results from phase II study of RA-101495 in PNH

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Topline phase IIa results reported from IW-1973 studies

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FDA grants orphan drug status to Seres' microbiome therapeutic candidate

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CKD273 biomarker panel predicts mortality in patients with diabetic nephropathy

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Zebrafish model illuminates role of TTN gene variants in dilated cardiomyopathy

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BL-8040 plus high-dose Ara-C improves overall survival in phase IIa study in r/r AML

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FDA gives orphan drug designation to SHP-647 for pediatric ulcerative colitis

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Lilly initiates phase I study of LY-3381916 alone and in combination with LY-3300054 in solid tumors

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Pembrolizumab shows promise for drug-resistant gestational trophoblastic neoplasia

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Burosumab shows positive results in phase III study in X-linked hypophosphatemia

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ViiV Healthcare UK patents novel HIV integrase inhibitors

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La Jolla Pharmaceutical initiates pivotal study of LJPC-401 in patients with beta thalassemia

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Mustang Bio signs agreements with Harvard and Beth Israel Deaconess in cancer immunotherapy

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Mirati Therapeutics and Array BioPharma describe new mutant KRAS inhibitors

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Montreal Neurological Institute and Takeda Canada enter ALS research agreement

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Evotec and Ncardia in licensing agreement for stem cell derived cellular disease modeling IP

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Roche identifies novel compounds for hepatitis B virus infection

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Probiodrug and Crossbeta extend strategic partnership in Alzheimer's biomarkers

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Glenmark Pharmaceuticals identifies new nuclear receptor ROR-gamma antagonists

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Tioga reports reduced nighttime itching in asimadoline study in atopic dermatitis

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Foresee completes phase I studies of MMP-12 inhibitor FP-025

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SymBio announces termination of license agreement with The Medicines Company

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FDA issues new guidance on 3D printing

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