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FDA Approves Novartis Drug for Rare Kidney Disease TreatmentNovartis NVS announced that the FDA has ... the drug for the treatment of adults with C3 glomerulopathy (C3G) to reduce proteinuria. C3G is a progressive and ultra-rare kidney disease that is ...
On Thursday, the FDA granted accelerated approval to Novartis AG’s NVS Fabhalta ... at risk of rapid disease progression. In December 2023, the FDA approved Fabhalta as the first oral ...
March 21, 2025 – The FDA has approved a drug as the first ... according to a news release by Novartis, the drug's maker. A yearlong clinical trial involving adult patients with C3G sought ...
An ultra-rare kidney disease that ... now has its first FDA-approved therapy. The affirmative regulatory decision is the third for Novartis’s Fabhalta, building up the drug’s pipeline-in ...
IgAN, which is also called Berger’s disease, is an autoimmune kidney condition where ... according to a news release by Novartis, the drug’s maker. The FDA’s decision is based on 36 ...
Aug 7 (Reuters) - The U.S. Food and Drug Administration has approved the use of Novartis' (NOVN.S), opens new tab drug to reduce excess protein in the urine of patients with a type of kidney ...
This is the third US approval for Fabhalta and its second within the Novartis kidney disease portfolio since August 2024, when Fabhalta was granted accelerated approval by the FDA for the ...
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