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Vertex Announces FDA Approval for ORKAMBI (lumacaftor/ivacaftor) in Children With Cystic Fibrosis…

Sep 6, 2022
Vertex Pharmaceuticals Incorporated announced the U.S. Food and Drug Administration (FDA) approved expanded use of ORKAMBI (lumacaftor/ivacaftor) to include children with cystic…
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Imfinzi plus chemotherapy approved in the US as the first immunotherapy regimen for patients with…

Sep 6, 2022
AstraZeneca’s Imfinzi (durvalumab) has been approved in the US for the treatment of adult patients with locally advanced or metastatic biliary tract cancer (BTC) in combination with…
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AVA6000 receives Orphan Drug Designation from the US Food and Drug Administration

Sep 6, 2022
Avacta Group plc, a clinical stage oncology drug company and developer of powerful diagnostics based on its innovative Affimer and pre|CISION platforms, announces that the US Food and…
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FDA approves the first treatment option for generalized pustular psoriasis flares in adults

Sep 5, 2022
Boehringer Ingelheim announced the U.S. Food and Drug Administration has approved SPEVIGO, the first approved treatment option for generalized pustular psoriasis (GPP) flares in adults.…
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FDA approves the first treatment option for generalized pustular psoriasis flares in adults

Sep 2, 2022
Boehringer Ingelheim announced the U.S. Food and Drug Administration has approved SPEVIGO, the first approved treatment option for generalized pustular psoriasis (GPP) flares in adults.…
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Cambrex Completes First Phase of $30 Million Capacity Expansion Project in High Point, North…

Sep 2, 2022
Cambrex announced the completion of the first phase of its $30 million investment in its small molecule active pharmaceutical ingredient (API) manufacturing facility in High Point,…
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ProofPilot Announces Partnership with Human API to Advance Patient Screening and Clinical Monitoring…

Sep 2, 2022
ProofPilot, the digital protocol automation platform for clinical trials, and Human API, the industry-leading platform enabling life sciences organizations to connect and convert…
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Maze Therapeutics Announces FDA Orphan Drug Designation Granted to MZE001 for the Treatment of Pompe…

Sep 2, 2022
Maze Therapeutics, a company translating genetic insights into new precision medicines, today announced that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug…
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Novavax Nuvaxovid COVID-19 Vaccine Recommended by CHMP for Expanded Conditional Marketing…

Sep 2, 2022
Novavax, Inc. announced that Nuvaxovid (NVX-CoV2373) COVID-19 vaccine has been recommended for expanded conditional marketing authorization (CMA) in the European Union (EU) as a…
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Novo Nordisk to acquire Forma Therapeutics and expand presence in sickle cell disease and rare blood…

Sep 2, 2022
Novo Nordisk and Forma Therapeutics, Holdings Inc. announced that they have entered into a definitive agreement under which Novo Nordisk will acquire Forma Therapeutics for USD 20 per…
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Press Releases

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