Clinical Trial SuccessNXC-201 demonstrated a 75% hematologic complete response rate in the NEXICART-2 trial for r/r AL amyloidosis.
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.
Regulatory Approval OutlookAnalyst increased the probability of approval for NXC-201 in r/r AL amyloidosis to 85%, up from the prior 40%.