Clinical Trial SuccessNEXICART-2 trial results show a 100% response rate and a 70% hematologic complete response rate for NXC-201 in treating r/r AL amyloidosis, with no relapse or progression observed.
Market OpportunityThere are currently no FDA-approved agents available for treatment of r/r AL amyloidosis, indicating a potential market opportunity for Immix's treatment.
Safety ProfileNo patients experienced Grade 3 or higher cytokine release syndrome or neurotoxicity events in the NEXICART-2 trial, indicating a favorable safety profile.