News

Novartis 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 ...
Novartis NVS obtains FDA ... disease. Approximately 50% of patients with persistent proteinuria progress to kidney failure within 10 to 20 years of diagnosis. The approval Vanrafia marks the third ...
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 ...
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 ...
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 ...
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 ...
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 ...