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BioWorld - Friday, December 5, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

June 1, 2017

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Novel Drosophila FXS model as promising screening strategy for therapeutic discovery

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EpimAb Biotherapeutics and WuXi Biologics collaborate to advance development of EMB-01

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Advaxis and BMS to test ADXS-DUAL plus Opdivo in metastatic cervical cancer

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Sylentis initiates phase III HELIX study of SYL-1001as treatment of dry eye syndrome

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Researchers design a novel antibody-powered DNA-based nanomachine

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ProQR Therapeutics receives FDA fast track designation for QR-110

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EMA's COMP recommends orphan medicinal product designation for Catalyst Biosciences' CB-2679d

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Alnylam's givosiran receives FDA breakthrough therapy designation

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IMIDomics enters strategic collaboration with Celgene

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Eisai and Johns Hopkins announce extension of their drug discovery collaboration

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Phase III HALO study of fremanezumab in migraine meets endpoints

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FDA grants rare pediatric disease designation to Amicus' SD-101 for epidermolysis bullosa

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New model reveals role of IRAK-M in rhinovirus infection

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AstraZeneca presents serine-protein kinase ATM inhibitors

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FDA grants priority review to Vyxeos NDA for AML

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FDA approves Novo Nordisk's Rebinyn for hemophilia B

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Roche divulges equilibrative nucleoside transporter 1 inhibitors

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MabVax enters research agreement with Memorial Sloan Kettering for CAR T-cell therapeutics

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Simon Fraser University and collaborator discover MRSA pyruvate kinase inhibitors

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FDA approves first topical ocular formulation of cetirizine

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R-Pharm CJSC presents MEK1/2 inhibitors

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Phase III study of elafibranor in NASH recommended to continue by DSMB

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Servier and ILTOO Pharma enter license agreement for ILT-101

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Janssen Pharmaceutica discloses PDE2 inhibitors

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FDA, EMA accept Pfizer's applications seeking to expand approved use of Sutent

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Review committee recommends dose escalation in MEI Pharma's phase I study of ME-401

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Minerva Neurosciences to amend MIN-202 agreement with Janssen

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First patient enters Oncology Venture's phase I/II study of APO-010

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Transient improvement seen in children with autism treated with suramin

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FAM46A mutations found to cause a form of osteogenesis imperfecta

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