The approval of iptacopan in reducing proteinuria in adult patients with native kidney C3G was based on data from the randomized, double-blind, placebo-controlled, phase 3 APPEAR-C3G trial.
DelveInsight's "EMPAVELI Market Size, Forecast, and Market Insight Report" highlights the details around EMPAVELI, a ...
Novartis' Fabhalta has become the first treatment approved by the FDA for the ultra-rare kidney disease C3G. But analysts ...
Basel, March 20, 2025 – Novartis today announced that oral Fabhalta ® (iptacopan) has received U.S. Food and Drug Administration (FDA) approval for the treatment of adults with C3 glomerulopathy (C3G) ...
Novartis' Fabhalta receives FDA approval for C3 glomerulopathy, expanding its kidney disease portfolio as global regulatory ...
ARO-C3 is designed to reduce hepatocyte production of complement C3 as a potential ... stage studies Effects on proteinuria (too much protein in the urine): The mean reduction in spot UPCR was ...
Both are markers of alternative pathway complement activity ... improved with a 41% reduction in spot [urine protein-to-creatinine ratio].” ARO-C3 is one of Arrowhead’s earliest-stage ...
which can generate improved or novel molecules to help correct disease-causing imbalances in the complement and coagulation systems (Fig. 1). Proteases cleave or degrade proteins with high ...
therapeutic designed to reduce liver production of complement component 3 (C3) as a potential therapy for various complement mediated diseases. The company plans to present additional results at a ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results