Clinical Trial ResultsUpdated results from the NEXICART-1 trial show NXC-201 elicited a 94% overall response rate (ORR) and a 75% complete response (CR) rate in 16 patients.
Market PotentialAnalysts forecast peak global NXC-201 sales of approximately $525M, given the lack of FDA-approved agents for relapsed/refractory AL amyloidosis and NXC-201's initial clinical data.
Regulatory MilestonesThe FDA granted RMAT designation to NXC-201, which is being evaluated in NEXICART-2 trial for the treatment of relapsed/refractory AL Amyloidosis.