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Gilead Announces First Global Regulatory Approval of Sunlenca (Lenacapavir), the Only Twice-Yearly…

Aug 23, 2022
Gilead Sciences, Inc. announced that the European Commission (EC) has granted Marketing Authorization for Sunlenca (lenacapavir) injection and tablets for the treatment of HIV…
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Ocelot Bio Receives FDA Orphan Drug Designation for OCE-205 for the Treatment of Hepatorenal…

Aug 23, 2022
Ocelot Bio, Inc., a clinical-stage biopharmaceutical company focused on the development of innovative therapeutics to treat complications of end-stage liver disease (ESLD), announced…
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Porton Advanced Solutions completes a Series B financing round to expand its end-to-end Gene and…

Aug 22, 2022
On August 19, 2022, Porton Advanced Solutions (Porton Advanced) announced the completion of its Series B financing round with over US$80Million. Current round of financing was led by…
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Invitation from the Aseptic Processing Conference Chairman James Drinkwater at F Ziel

Aug 22, 2022
SAE Media Group reports: James Drinkwater is chairing the 2nd Annual Aseptic Processing Conference, taking place on 19–20 September 2022, in London, UK. SAE Media Group proudly…
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Bristol Myers Squibb Completes Acquisition of Turning Point Therapeutics, Expanding Precision…

Aug 19, 2022
Bristol Myers Squibb announced that it has successfully completed its acquisition of Turning Point Therapeutics, Inc. (“Turning Point”), in an all-cash transaction. With the completion…
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FDA Accepts Astellas’ New Drug Application for Fezolinetant

Aug 19, 2022
Astellas Pharma Inc. announced that the U.S. Food and Drug Administration (FDA) has accepted the company's New Drug Application (NDA) for fezolinetant, an investigational oral,…
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Atomwise Signs Strategic Multi-Target Research Collaboration with Sanofi for AI-Powered Drug…

Aug 19, 2022
Atomwise announced that it has established a strategic and exclusive research collaboration with Sanofi that will leverage its AtomNet platform for computational discovery and research…
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European Commission Approves Celltrion Healthcare’s Vegzelma (CT-P16, biosimilar bevacizumab) for…

Aug 19, 2022
Celltrion Healthcare announced that the European Commission (EC) has approved Vegzelma (CT-P16), a biosimilar bevacizumab referencing EU-approved Avastin, for the treatment of…
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Nuance Pharma Announces Clearance of IND Application for Ensifentrine Pivotal Clinical Trials for…

Aug 18, 2022
Nuance Pharma announces the Center for Drug Evaluation has approved its Investigational New Drug application supporting its pivotal clinical trial of Ensifentrine for the maintenance…
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Valneva Initiates Rolling Submission of FDA Biologics License Application for its Single-Shot…

Aug 18, 2022
Valneva SE announces that it has initiated rolling submission of the Biologics License Application (BLA) to the U.S. Food and Drug Administration (FDA) seeking approval of the Company’s…
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