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BioWorld - Thursday, December 18, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Dec. 20, 2017

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DelSiTech and C-TRI to jointly develop long-acting controlled release formulations

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Bioharmony Therapeutics receives support to develop lysins for bacterial infections

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BeiGene begins phase II study of pamiparib

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Twin epigenetic study reveals idiopathic epilepsy biomarkers

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Array BioPharma and Pfizer to jointly test several cancer drug combinations

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Shire reports topline results from phase II/III study of SHP-609

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Pilot clinical study of Aclaris Therapeutics' ATI-50002 in vitiligo begins

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REGENXBIO's IND for study of RGX-121 in MPS II now active

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Elacestrant significantly reduced FES uptake in patients with ER+/HER2- breast cancer

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Bispecific antibody targeting [90Y]-DOTA and CD45 may enhance radiotherapy for leukemia

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Critical Outcome Technologies' COTI-2 safe, well tolerated in phase I study

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FDA gives fast track designation to Ovid Therapeutics' OV-101 for Angelman syndrome

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Novel P2X3 and/or P2X2/3 receptor antagonists identified at Shionogi

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First patient screened in Minerva Neurosciences' phase III study of MIN-101

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GlycoMimetics patents novel E-selectin binding inhibitors

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BioMarin initiates first phase III study of valoctocogene roxaparvovec for severe hemophilia A

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Transcriptx presents nucleic acids encodingdynein intermediate chain 1, axonemal

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Updated phase II data for tetrathiomolybdate in patients with breast cancer at risk for recurrence

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FDA approves Luxturna gene therapy for biallelic RPE65 mutation-associated retinal dystrophy

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Faron Pharmaceuticals cleared to continue INFORAAA study of Traumakine

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FDA approves Cabometyx for previously untreated advanced RCC

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Second Genome's lead candidate demonstrates safety, tolerability in phase I study

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Solid Biosciences initiates phase I/II study of SGT-001 in Duchenne muscular dystrophy

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Otsuka and X-Chem sign collaborative research agreement

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Onconova and HanX enter license and collaborative development agreement for ON-123300

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FDA approves Prexxartan

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Promising results for novel anti-EGFR radiotracer in patients with non-small cell lung cancer

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FDA accepts for review BLA for Samsung Bioepis' trastuzumab biosimilar

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FDA approves Bosulif for newly diagnosed Ph+ CML

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Biogen and Ionis enter new collaboration for SMA

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