Biopharma Transcript

Immix Biopharma, Inc. IMMX

Nasdaq · Phase 2 · hematology · cell therapy · EDGAR · Updated Oct 24, 2026

Immix Biopharma, Inc. (Nasdaq: IMMX) is a hematology drug developer. Its lead program, NXC-201 (CAR-T), is in Phase 2 for relapsed/refractory AL amyloidosis. Its next catalyst on record is NXC-201: NEXICART-2 final readout followed by BLA submission (date not stated).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Next further out: NXC-201 — NEXICART-2 final readout followed by BLA submission (date not stated). 2 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
NXC-201 (NEXICART-2, US Phase 1b/2)relapsed/refractory AL amyloidosiscell therapyPhase 2
NXC-201 (NEXICART-1, ex-US Phase 1b/2a)relapsed/refractory AL amyloidosiscell therapyPhase 2
NXC-201 newly diagnosed AL amyloidosis (planned randomized Phase 3)newly diagnosed AL amyloidosiscell therapyPre-clinical
Other NXC-201 indications and preclinical candidates—cell therapyPre-clinical

Recent results and decisions

  1. Sep 29, 2026
    n/a Immix Biopharma priced underwritten public offering of 11,363,637 shares of common stock at $11.00 per share for expected net proceeds of approximately $117.1 million.The Company estimates that the net proceeds to the Company from the Offering, after deducting underwriting discounts and commissions, and estimated offering expenses, are expected to be approximately $117.1 million. Filing
  2. Mar 30, 2026
    completed enrollment Enrollment completed in the 40-patient registrational Phase 2 NEXICART-2 trial of CAR-T NXC-201, per prior guidance.Immix Biopharma, Inc. today announced that NEXICART-2 enrollment is complete, meeting Company guidance, with topline results expected in Q3 2026, followed by BLA submission and planned commercial launch. Filing

For subscribers

Other phase 2 hematology companies