Press Releases October 5, 2026 08:45 AM

Immix Biopharma to Participate in the 45th Annual J.P. Morgan Healthcare Conference

Immix Biopharma to Present at 45th Annual J.P. Morgan Healthcare Conference, Showcasing Lead CAR-T Therapy for AL Amyloidosis

By Derek Hwang
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IMMX

Immix Biopharma, a Nasdaq-listed company specializing in AL Amyloidosis treatment, announced its participation in the upcoming J.P. Morgan Healthcare Conference. The company will present data on its lead CAR-T cell therapy candidate, NXC-201, designed to target and eliminate toxic light chains causing organ failure in AL Amyloidosis patients. NXC-201 is in a potentially registrational U.S. clinical trial and has received multiple FDA and EMA designations that recognize its therapeutic promise.

Immix Biopharma to Participate in the 45th Annual J.P. Morgan Healthcare Conference
IMMX
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Key Points

  • Immix Biopharma will present at the 45th Annual J.P. Morgan Healthcare Conference in January 2027.
  • NXC-201, the lead CAR-T cell therapy candidate, targets BCMA and includes proprietary technology to reduce non-specific activation and improve efficacy.
  • NXC-201 is in a U.S. multicenter trial (NEXICART-2) for relapsed/refractory AL Amyloidosis with breakthrough and orphan drug designations granted by FDA and EMA.
  • The participation highlights Immix's leadership in a niche and severe disease area, pointing to near-term data readouts and regulatory milestones.

LOS ANGELES, CA, Oct. 05, 2026 (GLOBE NEWSWIRE) -- Immix Biopharma, Inc. (“ImmixBio”, “Company”, “We” or “Us” or ”IMMX”), a global leader in AL Amyloidosis, today announced that it will present at the 45th Annual J.P. Morgan Healthcare Conference being held January 11-14, 2027 in San Francisco, CA.

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 a global leader in 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 proprietary CD3ζ, CD8 hinge and binder “digital filter” 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 potentially 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

  • Clinical trial outcomes for NXC-201 remain uncertain and could negatively impact the company if results are poor or delayed.
  • Regulatory approval, despite breakthrough and orphan designations, is not guaranteed and may face hurdles.
  • Market adoption and commercial success depend on competitive landscape dynamics and reimbursement for a rare disease therapy.

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