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Maroc Maroc - ZACKS.COM - All Stories - 21/Mar 18:10

FDA Approves Novartis Drug for Rare Kidney Disease Treatment

Novartis wins FDA approval for the label expansion of Fabhalta for a third indication - treatment of adults with C3 glomerulopathy.

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FDA Approves Novartis Drug for Rare Kidney Disease Treatment

zacks.com - 21/Mar 18:10

Novartis wins FDA approval for the label expansion of Fabhalta for a third indication - treatment of adults with C3 glomerulopathy.

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FDA Approves Tremfya for Active Crohn Disease in Adults

drugs.com - 24/Mar 21:40

MONDAY, March 24, 2025 -- The U.S. Food and Drug Administration has approved Tremfya (guselkumab) for adult patients with moderately to severely...

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FDA Approves Blujepa (gepotidacin) for the Treatment of Uncomplicated Urinary Tract Infections

drugs.com - 25/Mar 18:03

London, UK -- 25 March 2025 -- GSK plc (LSE/NYSE: GSK) today announced that the US Food and Drug Administration (FDA) has approved Blujepa...

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Alnylam Gets FDA Nod for Expanded Use of Amvuttra in Cardiomyopathy

zacks.com - 21/Mar 16:46

ALNY secures FDA approval for an sNDA in the United States, seeking the label expansion of Amvuttra to treat ATTR amyloidosis with cardiomyopathy.

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Alnylam Gets FDA Nod for Expanded Use of Amvuttra in Cardiomyopathy

zacks.com - 21/Mar 16:46

ALNY secures FDA approval for an sNDA in the United States, seeking the label expansion of Amvuttra to treat ATTR amyloidosis with cardiomyopathy.

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FDA Approves Vykat XR (diazoxide choline) to Treat Hyperphagia in Prader-Willi Syndrome

drugs.com - 26/Mar 02:03

REDWOOD CITY, Calif., March 26, 2025 (GLOBE NEWSWIRE) -- Soleno Therapeutics, Inc. (NASDAQ: SLNO), a biopharmaceutical company developing novel...

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J&J's Tremfya Gets FDA Nod for 2nd IBD Condition Crohn's Disease

zacks.com - 21/Mar 12:28

FDA approves J&J's Tremfya for its fourth indication and the second IBD condition.

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J&J's Tremfya Gets FDA Nod for 2nd IBD Condition Crohn's Disease

zacks.com - 21/Mar 12:28

FDA approves J&J's Tremfya for its fourth indication and the second IBD condition.

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Exelixis Announces U.S. FDA Approval of Cabometyx (cabozantinib) for Patients with Previously Treated Advanced Neuroendocrine Tumors

drugs.com - 26/Mar 19:03

ALAMEDA, Calif.--(BUSINESS WIRE)--Mar. 26, 2025-- Exelixis, Inc. (Nasdaq: EXEL) today announced that the U.S. Food and Drug Administration (FDA) has...

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ABT Stock to Gain From FDA IDE Approval for Its Coronary IVL System

zacks.com - 25/Mar 13:16

Abbott's Coronary IVL System wins FDA IDE nod, offering a potential new treatment for arterial calcium blockages.