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BioWorld - Monday, December 8, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Jan. 4, 2017

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Medsenic's arsenic trioxide awarded E.U. orphan drug designation for GvHD, begins phase II trial

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Novel prototypical peptidomimetic inhibitor demonstrates efficacy in models of AML

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IMPDH inhibition as a promising new therapeutic strategy against MLL-fusion leukemia

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AMPK identified as a novel therapeutic target in acute lymphoblastic leukemia

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Researchers identify a novel target for AML and MDS

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Xenikos obtains funding to support T-Guard development

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Flamel Technologies now Avadel Pharmaceuticals

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Axsome Therapeutics cleared to begin phase II/III study of AXS-05 in Alzheimer's

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Bayer Pharma patents muscarinic acetylcholine M2 receptor PAMs

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University of Florida discloses aminoacyl-tRNA synthetase inhibitors

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Zynerba Pharmaceuticals commences FAB-C study of ZYN-002 gel

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Abeona Therapeutics' ABO-201 granted orphan drug designation in Europe

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Inventiva initiates patient enrollment in phase IIb study of IVA-337

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Almirall describes JAK inhibitors

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Soliqua available in U.S.

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Adhaere Pharmaceuticals presents anticancer agents

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Kite Pharma submits IND for phase I study of KITE-718

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GSK closes agreement to divest non-core assets to Aspen

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FDA grants priority review to Stivarga sNDA for hepatocellular carcinoma

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Astellas Pharma discloses dopamine D1 receptor PAMs

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Seattle Genetics presents new clinical data for vadastuximab talirine

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Agile reports phase III topline results for Twirla hormonal contraceptive patch

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Newron Pharmaceuticals reports promising results for evenamide in schizophrenia

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Inspyr Therapeutics to study mipsagargin combination therapies

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NewVac's phase II study of quisinostat meets primary endpoints

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Inotek reports topline results from pivotal trial of trabodenoson for glaucoma

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Acura explores financing and strategic alternatives

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CymaBay Therapeutics signs license agreement with Kowa for arhalofenate in U.S.

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Cellectis submits IND to begin phase I trials of UCART-123

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