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 ...
The FDA’s new approval makes the drug the first GLP-1 treatment option for people with type 2 diabetes and chronic kidney disease. "Chronic kidney disease is very serious and common in patients ...
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 U.S. Food and Drug Administration ... within the Novartis kidney disease portfolio since August 2024, when Fabhalta was granted accelerated approval by the FDA for the reduction ...
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 ...
Novartis NVS announced that the FDA has approved Fabhalta (iptacopan) for a third indication. The regulatory body approved the drug for the treatment of adults with C3 glomerulopathy (C3G) to reduce ...