Immix Biopharma prices $125M stock offering at $11.00 per share
- Immix Biopharma priced a $125 million underwritten stock offering on September 29, 2026
- The company sold 11,363,637 shares at a price of $11.00 per share
- Net proceeds will fund development of lead candidate NXC-201 and general corporate purposes
- J.P. Morgan served as the sole book-running manager for the deal

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Immix Biopharma (NASDAQ: IMMX) priced a $125 million underwritten registered offering of common stock on September 29, 2026. The company sold 11,363,637 shares at a public offering price of $11.00 per share.
The gross proceeds are expected to be $125 million before deducting underwriting discounts, commissions, and offering expenses payable by the company. Immix intends to use the net proceeds to fund the development of its lead candidate, NXC-201, as well as for working capital and general corporate purposes. The offering is expected to close on or about September 30, 2026, subject to customary closing conditions.
Offering details
The transaction was structured as an underwritten registered offering pursuant to a shelf registration statement on Form S-3 filed with the U.S. Securities and Exchange Commission (SEC). J.P. Morgan served as the sole book-running manager for the deal.
| Metric | Value |
|---|---|
| Shares Sold | 11,363,637 |
| Price Per Share | $11.00 |
| Gross Proceeds | $125 million |
| Closing Date | On or about September 30, 2026 |
Investor participation
The offering attracted participation from both new and existing institutional investors. Key participants included Eventide Asset Management, Janus Henderson Investors, Ridgeback Capital Investments L.P., and Wellington Management. Other leading U.S. biotechnology institutional investors and mutual funds also participated in the round.
Strategic context
Immix Biopharma is a global leader in treating relapsed/refractory AL Amyloidosis, a disease where toxic light chains cause organ failure. Its lead candidate, NXC-201, is a sterically-optimized BCMA-targeted CAR-T cell therapy currently being evaluated in the U.S. multi-center NEXICART-2 study. The therapy has received Breakthrough Therapy Designation and Regenerative Medicine Advanced Therapy designation from the FDA, along with Orphan Drug Designation from both the FDA and the European Medicines Agency.
How will the dilution from the 11.36 million new shares impact Immix Biopharma's stock price trajectory in the immediate post-offering period?
What specific enrollment milestones for the NEXICART-2 study are expected to be achieved with the $125 million in net proceeds?
Given the Breakthrough Therapy Designation, what is the anticipated timeline for submitting an NDA or BLA for NXC-201?




























