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BioWorld - Saturday, June 6, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

July 24, 2017

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EMA's CHMP grants positive opinion for dupixent for the treatment of atopic dermatitis

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FDA grants clearance to first neonatal magnetic resonance imaging device

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DNA vaccines targeting alpha-synuclein show promise for the treatment of dementia

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EMA committee backs approval of Janssen's Symtuza

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FDA gives orphan drug exclusivity to CSL Behring's Haegarda

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FDA approves new self-injectable formulation of Benlysta

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FDA awards fast track designation to Valneva's Lyme disease vaccine candidate VLA-15

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AbbVie's Humira receives positive opinion from EMA for uveitis

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Phase I PK/PD data presented for Eisai's PDE9A inhibitor E-2027

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Lutathera receives positive opinion from EMA for GEP-NETs

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GSK and Innoviva seek E.U. approval of extended use of Relvar Ellipta

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Chugai files for Japanese approval of emicizumab in hemophilia A

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ORIC Pharmaceuticals presents glucocorticoid receptor antagonists

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Council of Scientific and Industrial Research divulges compounds for vitiligo treatment

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CHMP supports approval of Novartis' Rydapt in E.U.

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Chiesi Farmaceutici discloses MAPK14 inhibitors

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Xermelo obtains positive opinion from EMA committee

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NeuroDerm to be acquired by Mitsubishi Tanabe Pharma

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Cancer Research Technology discovers TTK inhibitors

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CHMP grants positive opinion for Keytruda in urothelial carcinoma

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Sichuan Haisco Pharmaceutical discovers compounds for asthma treatment

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CHMP recommends approval of avelumab for metastatic Merkel cell carcinoma

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CHMP issues negative opinion on Vanda Pharmaceuticals' Fanaptum

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EMA committee issues new Day 180 list of outstanding issues for abaloparatide

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Tissue Regenix to acquire CellRight Technologies

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Identified a rare variant in ADAM17 gene tied to familial Alzheimer's disease

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EMA's CHMP recommends approval of Gazyvaro for previously untreated advanced follicular lymphoma

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EMA committee recommends approvals for Tecentriq in NSCLC and metastatic urothelial carcinoma

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RoActemra recommended for approval in E.U. for giant cell arteritis

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