Immix Biopharma Announces Pricing of Upsized $100 Million Underwritten Offering of Common Stock and Pre-Funded Warrants
Rhea-AI Summary
Immix Biopharma (NASDAQ:IMMX) priced an underwritten offering of 19,117,646 common shares at $5.10 each and pre-funded warrants to purchase 490,196 shares at $5.09 per warrant, for expected gross proceeds of $100 million.
The offering is expected to close on or about December 9, 2025, subject to customary closing conditions. Immix intends to use net proceeds to fund NXC-201 development, working capital and general corporate purposes, and says cash plus expected CIRM grant disbursements should fund operations into mid-2027. Morgan Stanley is sole book-runner; Citizens Capital Markets and Mizuho are co-managers. Securities are offered under a Form S-3 shelf registration.
Positive
- $100 million gross proceeds expected from the offering
- Proceeds earmarked to fund NXC-201 development
- Company expects runway into mid-2027 including CIRM grant
Negative
- 19,607,842 total shares/warrants issued may dilute shareholders
- Closing is subject to customary conditions, not guaranteed
Key Figures
Market Reality Check
Peers on Argus
IMMX gained 13.93% while peers showed mixed, more modest moves (e.g., BYSI +5.29%, OSTX +1.59%, ACET -0.15%, IGMS -2.31%, NRXP -2.48%). This points to a stock-specific reaction rather than a broad biotech rotation.
Historical Context
| Date | Event | Sentiment | Move | Catalyst |
|---|---|---|---|---|
| Nov 12 | Executive appointment | Positive | +15.2% | Hired Chief Commercial Officer to lead planned NXC-201 U.S. launch. |
| Nov 03 | Clinical data update | Positive | -4.2% | Interim NEXICART-2 trial results selected for ASH 2025 oral presentation. |
| Oct 14 | Conference participation | Neutral | -0.8% | Participation and meetings at Guggenheim Healthcare Innovation Conference. |
| Oct 06 | Conference abstract | Positive | +9.0% | NXC-201 abstract accepted for presentation at ASH 2025 annual meeting. |
| Oct 01 | Conference participation | Neutral | -0.5% | Planned presentation and meetings at Piper Sandler Healthcare Conference. |
Recent news has mostly seen aligned price reactions, with one notable divergence on positive clinical communication.
Over the last few months, Immix Biopharma has focused on advancing and positioning NXC-201. On Nov 12, 2025, the company appointed a Chief Commercial Officer to lead the U.S. launch, and the stock rose 15.17%. Earlier, interim NEXICART-2 data selected for an ASH 2025 oral presentation on Nov 3, 2025 coincided with a -4.21% move. Multiple conference and ASH abstract announcements in October produced relatively modest moves between about -0.8% and +8.98%. Against this backdrop, the current capital raise follows a period of strong clinical and commercial setup activity.
Regulatory & Risk Context
The company has an active Form S-3 shelf registration dated 2025-10-06, expiring on 2028-10-06. The provided excerpt details holders and offering-related expenses of $20,000 each for legal and accounting and total offering costs of $46,977, but does not specify the shelf size. The shelf is noted as not effective in the context data and has 0 recorded usages before this underwritten offering.
Market Pulse Summary
This announcement details a sizable equity and pre-funded warrant financing totaling $100 million, priced at $5.10 per share and $5.09 per pre-funded warrant, to support NXC-201 and general operations. It follows recent filings showing a Q3 net loss of $7.59 million and cash of $15.95 million alongside going concern language. Investors may track use of proceeds, NXC-201 clinical milestones, and future use of the Form S-3 shelf registration when assessing dilution and funding risk.
Key Terms
pre-funded warrants financial
shelf registration statement regulatory
form s-3 regulatory
prospectus supplement regulatory
book-running manager financial
AI-generated analysis. Not financial advice.
LOS ANGELES, CA, Dec. 07, 2025 (GLOBE NEWSWIRE) -- Immix Biopharma, Inc. (“ImmixBio”, “Company”, “We” or “Us” or ”IMMX”), a global leader in relapsed/refractory AL Amyloidosis, today announced the pricing of an underwritten registered offering of 19,117,646 shares of its common stock at a price to the public of
Immix intends to use the net proceeds from this offering, together with its existing cash and cash equivalents to fund NXC-201 development and for working capital and general corporate purposes. Immix believes that the net proceeds from the offering, together with its existing cash and cash equivalents, and expected disbursements under the Company’s CIRM grant will be sufficient to meet the Company’s operational needs into mid-2027.
Morgan Stanley is acting as the sole book-running manager for the offering. Citizens Capital Markets and Mizuho are acting as co-managers for the offering.
The securities in the registered offering are being offered and sold pursuant to a “shelf” registration statement on Form S-3 (File No. 333-269100), including a base prospectus, filed with the U.S. Securities and Exchange Commission (the “SEC”) on January 3, 2023, and declared effective on January 11, 2023. A prospectus supplement and accompanying prospectus describing the terms of the registered offering will be filed with the SEC and will be available on its website at www.sec.gov. Copies of the prospectus supplement and the accompanying prospectus relating to the offering, when available, may also be obtained from: Morgan Stanley & Co. LLC, attention: Prospectus Department, 180 Varick Street, 2nd Floor, New York, New York 10014, by phone: 1-866-718-1649 or by email: prospectus@morganstanley.com.
This press release shall not constitute an offer to sell or the solicitation of an offer to buy any of the securities described herein, nor shall there be any sale of these securities in any state or jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction.
About Immix Biopharma, Inc.
Immix Biopharma, Inc. (ImmixBio) (Nasdaq: IMMX) is a 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 Regenerative Medicine Advanced Therapy (RMAT) by the US FDA and Orphan Drug Designation (ODD) by FDA and in the EU by the EMA.
Forward Looking Statements
This press release contains forward-looking statements regarding Immix Biopharma, Inc., its results of operations, prospects, future business plans and operations and the matters discussed above, including, but not limited to, statements relating to the offering, including the timing of the closing of the offering, the anticipated use of proceeds therefrom, the Company’s cash runway, the potential benefits of our product candidate CAR-T NXC-201 and the timing and results related to clinical trials. These statements involve risks and uncertainties, and actual results may differ materially from any future results expressed or implied by the forward-looking statements. Forward-looking statements also include, but are not limited to, our plans, objectives, expectations and intentions and other statements that contain words such as “expects”, “contemplates”, “anticipates”, “plans”, “intends”, “believes”, “estimates”, “potential”, and variations of such words or similar expressions that convey the uncertainty of future events or outcomes, or that do not relate to historical matters. Those forward-looking statements involve known and unknown risks, uncertainties and other factors that could cause actual results to differ materially. Among those factors are: (i) the risk that the further data from the ongoing Phase 1/2 clinical trials for CAR-T NXC-201 will not be favorably consistent with the data readouts to date, (ii) the risk that the Company may not be able to continue the NEXICART-2 multi-site U.S. Phase 1/2 clinical trial; (iii) the risk that the Company may not be able to advance to registration-enabling studies for CAR-T NXC-201 or other product candidates, (iv) that success in early phases of pre-clinical and clinicals trials do not ensure later clinical trials will be successful; (v) that no drug product developed by the Company has received FDA pre-market approval or otherwise been incorporated into a commercial drug product, (vi) the risk that the Company may not be able to obtain additional working capital with which to continue the clinical trials for CAR-T NXC-201, or advance to the initiation of registration-enabling studies, for such product candidates as and when needed and (vii) those other risks disclosed in the section “Risk Factors” included in the Company’s Annual Report on Form 10-K filed with the SEC on March 25, 2025 and other periodic or current reports subsequently filed with the Securities and Exchange Commission. These reports are available at www.sec.gov. Immix Biopharma cautions that the foregoing list of important factors is not complete. Immix Biopharma cautions readers not to place undue reliance on any forward-looking statements. Immix Biopharma does not undertake, and specifically disclaims, any obligation to update or revise such statements to reflect new circumstances or unanticipated events as they occur, except as required by law. If we update one or more forward-looking statements, no inference should be drawn that we will make additional updates with respect to those or other forward-looking statements.
Contacts
Mike Moyer
LifeSci Advisors
mmoyer@lifesciadvisors.com
Company Contact
irteam@immixbio.com