Press Releases April 9, 2026 08:45 AM

Immix Biopharma to Participate in the Jefferies Global Healthcare Conference

Immix Biopharma to Present at Jefferies Global Healthcare Conference, Showcasing CAR-T Therapy for AL Amyloidosis

By Leila Farooq IMMX
Immix Biopharma to Participate in the Jefferies Global Healthcare Conference
IMMX

Immix Biopharma, a Nasdaq-listed company focused on relapsed/refractory AL Amyloidosis treatments, announced participation at the Jefferies Global Healthcare Conference in June 2026. The company will hold investor meetings and provide updates on its lead CAR-T cell therapy candidate, NXC-201, which has received FDA Breakthrough Therapy and RMAT designations.

Key Points

  • Immix Biopharma will engage with investors at the Jefferies Global Healthcare Conference in New York in June 2026.
  • Their lead product, NXC-201, is a BCMA-targeted CAR-T cell therapy designed for relapsed/refractory AL Amyloidosis.
  • NXC-201 holds significant regulatory designations including FDA Breakthrough Therapy, RMAT, and Orphan Drug Designations, indicating high potential for approval and unmet medical need.
  • The announcement highlights advances in biotech sector therapies targeting rare hematologic diseases.

LOS ANGELES, CA, April 09, 2026 (GLOBE NEWSWIRE) -- Immix Biopharma, Inc. (“ImmixBio”, “Company”, “We” or “Us” or ”IMMX”), the global leader in relapsed/refractory AL Amyloidosis, today announced that it will participate and host institutional investor meetings at the Jefferies Global Healthcare Conference being held June 2-4, 2026 in New York, NY.

The Company will be available for one-on-one meetings during the conference. Interested investors should contact their Jefferies representative to request meetings. A link to access the replay, when available, will be posted to the Immix website on the Presentation & Events page under the Investors section.

About Immix Biopharma, Inc.
Immix Biopharma, Inc. (ImmixBio) (Nasdaq: IMMX) is the global leader in relapsed/refractory AL Amyloidosis. AL Amyloidosis is a devastating disease where the immune system, that’s supposed to protect, instead produces toxic light chains, clogging up the heart, kidney and liver, causing organ failure and death. Our lead candidate is sterically-optimized BCMA-targeted chimeric antigen receptor T (CAR-T) cell therapy NXC-201 with a “digital filter” that is designed to filter out non-specific activation. NXC-201 teaches the immune system to recognize and eliminate the source of the toxic light chains. NXC-201 is being evaluated in the U.S. multi-center study for relapsed/refractory AL Amyloidosis NEXICART-2 (NCT06097832), with a registrational design. NXC-201 has been awarded Breakthrough Therapy Designation (BTD) and Regenerative Medicine Advanced Therapy (RMAT) by the US FDA and Orphan Drug Designation (ODD) by FDA and in the EU by the EMA.

Contacts
Mike Moyer
LifeSci Advisors
[email protected]

Company Contact
[email protected]


Risks

  • The clinical trial NEXICART-2 is ongoing, and final results for NXC-201’s efficacy and safety have yet to be established, posing developmental and regulatory risks.
  • Competition in the CAR-T therapy space and potential challenges in commercializing treatments for a rare disease may impact market acceptance and financial outcomes.
  • Regulatory approval processes, while aided by special designations, still carry uncertainties that could delay or limit product availability.

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