Loading...
Loading...
Browse all stories on DeepNewz
VisitFDA Approves Incyte's Niktimvo for Chronic GVHD
Aug 14, 2024, 10:09 PM
The U.S. Food and Drug Administration (FDA) has approved Incyte Corporation's drug, Niktimvo™ (axatilimab-csfr), for the treatment of chronic graft-versus-host disease (GVHD). This condition is a potentially fatal complication that can occur after a stem cell transplant. The approval marks a significant advancement in the treatment options available for patients suffering from chronic GVHD. The drug, developed in collaboration with Syndax Pharmaceuticals, offers a new therapeutic option for managing this serious condition.
View original story
Markets
Yes • 50%
No • 50%
Publicly available information from Incyte Corporation's announcements or FDA updates
No • 50%
Yes • 50%
Publicly available information from European Medicines Agency (EMA) announcements
Yes • 50%
No • 50%
Publicly available stock price data from financial markets
Less than 10% • 25%
More than 30% • 25%
20% to 30% • 25%
10% to 20% • 25%
Publicly available market research reports and financial statements from Incyte
Other • 25%
Niktimvo • 25%
Jakafi • 25%
Pemazyre • 25%
Publicly available financial statements from Incyte Corporation
Bristol-Myers Squibb • 25%
Novartis • 25%
Pfizer • 25%
Other • 25%
Publicly available market research reports and competitive analysis