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60° Pharmaceuticals (60P) receives priority review designation for Malaria Drug

Feb 8, 2018
60 Degrees Pharmaceuticals (60P) received Priority Review Designation from the United States Food and Drug Administration (USFDA) for Tafenoquine (TQ) for prevention of malaria in…
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Concept Life Sciences expands GXP compliance

Feb 8, 2018
Concept Life Sciences announced the completion of the first phase of its GXP compliance plan, achieving GLP (good laboratory practice) accreditation of its Dundee site for in vitro …
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Novo Nordisk Launches Rebinyn in the United States for People with Hemophilia B

Feb 8, 2018
Novo Nordisk announced that Rebinyn, Coagulation Factor IX (Recombinant), GlycoPEGylated, is now available in the United States for the treatment of hemophilia B. Rebinyn is an…
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Sosei Provides an Update on Its Immuno-Oncology Clinical Program with AstraZeneca

Feb 8, 2018
Sosei Group Corporation announces that its immuno-oncology collaboration with AstraZeneca is progressing well. The first patient has been dosed in an expansion cohort in the Phase 1b…
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Selvita appoints Steffen Heeger as Chief Medical Officer

Feb 8, 2018
Selvita S.A. (WSE:SLV), a clinical stage drug discovery and development company focused on innovative medicines for oncology patients and drug discovery services, announced the…
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Major research project launched to crack aspirin’s anti-cancer properties

Feb 7, 2018
Cancer Research UK launches an international study to answer the final questions before aspirin could be recommended to reduce cancer risk. Studies have estimated that widespread…
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Roivant Sciences and ArQule enter into License Agreement for Derazantinib in China

Feb 7, 2018
Roivant Sciences and ArQule announced the initiation of a collaboration to pursue the development of derazantinib, a pan-FGFR (fibroblast growth factor receptor) inhibitor, in Greater…
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Xcovery initiates Phase 2 Clinical Trial for Ensartinib in Melanoma Patients with ALK Alternations

Feb 7, 2018
Xcovery announced the initiation of its Phase 2 clinical trial of ensartinib (X-396), the company’s lead anaplastic lymphoma kinase (ALK) drug candidate, in patients with advanced…
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Capricor receives FDA RMAT Designation for Duchenne Muscular Dystrophy Therapy

Feb 6, 2018
Capricor Therapeutics announced that the U.S. Food and Drug Administration (FDA) has granted CAP-1002, its lead investigational cell therapy for the treatment of Duchenne muscular…
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FDA Clears Oricula Therapeutics Investigational New Drug Application for Clinical Trials

Feb 6, 2018
ORICULA THERAPEUTICS, LLC., a biotech company introducing medications to preserve hearing and balance, announced FDA permission to begin volunteer human testing for safety,…
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