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

Key Takeaway: Immix Biopharma, Inc. will present at the 45th Annual J.P. Morgan Healthcare Conference from January 11-14, 2027, in San Francisco. The company is recognized for its work in AL Amyloidosis and is advancing its lead candidate, NXC-201, which has received Breakthrough Therapy Designation and other regulatory recognitions. A replay of the presentation will be available on the company's website.

Market Sentiment Analysis

POSITIVE FACTORS

  • Immix Biopharma is participating in a prestigious healthcare conference.
  • The company is a leader in AL Amyloidosis treatment.
  • NXC-201 has received multiple designations from the FDA, indicating strong potential.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+34%
120-day peak, hindsight
Typical move
7.5%
average across 3 past catalysts
Cash runway
~57 mo
Minimal dilution risk
Lead asset
NXC-201
Phase 3 · Light Chain (AL) Amyloidosis

Full Press Release Details

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 mmoyer@lifesciadvisors.com

Company Contact irteam@immixbio.com

Frequently Asked Questions

When is the J.P. Morgan Healthcare Conference?

The conference will be held from January 11-14, 2027.

What is NXC-201?

NXC-201 is Immix Biopharma's lead CAR-T cell therapy for AL Amyloidosis.

What designations has NXC-201 received?

NXC-201 has received Breakthrough Therapy Designation and RMAT from the FDA.

Where can I access the presentation replay?

The replay will be available on the Immix website under the Investors section.

Last updated: Oct 5, 2026