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CARVYKTI is the First and Only BCMA-Targeted Treatment Approved by the U.S. FDA for Patients with…

Apr 8, 2024
Johnson & Johnson announced that the U.S. Food and Drug Administration (FDA) has approved CARVYKTI (ciltacabtagene autoleucel; cilta-cel) for the treatment of adult patients with…
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Nurix Therapeutics Announces Extension of Strategic Collaboration with Gilead Sciences

Apr 3, 2024
Nurix Therapeutics, Inc., a clinical stage biopharmaceutical company developing targeted protein modulation drugs designed to treat patients with cancer and inflammatory diseases,…
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Solid Biosciences Receives Rare Pediatric Disease Designation from the FDA for Duchenne Muscular…

Apr 3, 2024
Solid Biosciences Inc., a life sciences company developing precision genetic medicines for neuromuscular and cardiac diseases, announced that the U.S. Food and Drug Administration (FDA)…
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Voydeya approved in the US as add-on therapy to ravulizumab or eculizumab for treatment of…

Apr 3, 2024
Voydeya (danicopan) has been approved in the US as add-on therapy to ravulizumab or eculizumab for the treatment of extravascular haemolysis (EVH) in adults with paroxysmal nocturnal…
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Trevi Therapeutics Adds Clinical Development Expertise in Chronic Cough to Leadership Team

Apr 3, 2024
Trevi Therapeutics, Inc., a clinical-stage biopharmaceutical company developing the investigational therapy Haduvio (oral nalbuphine ER) for the treatment of chronic cough in idiopathic…
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Eisai Completes Submission of LEQEMBI (lecanemab-irmb) Supplemental Biologics License Application…

Apr 2, 2024
Eisai Co., Ltd. and Biogen Inc. announced that Eisai submitted to the U.S. Food and Drug Administration (FDA) a Supplemental Biologics License Application (sBLA) for monthly…
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Gilead and Xilio Announce Exclusive License Agreement for Tumor-Activated IL-12 Program

Apr 1, 2024
Gilead Sciences, Inc. and Xilio Therapeutics, Inc. announced an exclusive license agreement to develop and commercialize Xilio’s Phase 1 tumor-activated IL-12 program, XTX301. Xilio…
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Eisai to Divest Rights for Merislon and Myonal in Japan to Kaken Pharmaceutical

Apr 1, 2024
Eisai Co., Ltd. announced that it has entered into an agreement to divest its rights for vertigo and equilibrium disturbance treatment Merislon (generic name: betahistine mesilate) and…
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FDA Approves EDURANT PED (rilpivirine) for Certain Pediatric Patients Living with HIV-1

Mar 21, 2024
Johnson & Johnsonannounced that the U.S. Food and Drug Administration (FDA) has approved EDURANT PED (rilpivirine) for the treatment of HIV-1 in combination with other…
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Lonza Signs Agreement to Acquire Large-Scale Biologics Site in Vacaville (US) from Roche

Mar 21, 2024
Lonza, a global manufacturing partner to the pharmaceutical, biotech and nutraceutical markets, announced it has signed an agreement to acquire the Genentech large-scale biologics…
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Press Releases

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