Immix Biopharma, Inc.

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IMMX

US45258H1068

Biotechnology & Medical Research

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Dec. 09	Immix Biopharma announces closing of upsized $100 million underwritten offering of common stock and pre-funded warrants	RE
Dec. 08	Immix Biopharma Prices $100 Million Offering	MT

Immix Biopharma Announces Positive Results for NXC-201 at ASCO Oral Presentation, Enabling Pathway to Best-In-Class Therapy for Relapsed/Refractory AL Amyloidosis

Published on 05/22/2025 at 04:02 pm EDT

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Immix Biopharma, Inc.

-6.08%

Immix Biopharma, Inc. announced publication of cell therapy NXC-201 Abstract #7508, selected for oral presentation at the 2025 American Society of Clinical Oncology Annual Meeting (ASCO 2025) being held in Chicago, Illinois. Immix's Phase 1/2 NEXICART-2 clinical trial is a U.S. multi-site, single-arm study to evaluate the efficacy and safety of NXC-201 in patients who are refractory to, or relapse on treatment for relapsed/refractory AL Amyloidosis. NEXICART-2 (NCT06097832) is an ongoing single-arm multi-site U.S. Phase 1/2 clinical trial of clinically-optimized CAR-T NXC-201 in relapsed/refractoryAL Amyloidosis.

Initial data from ex-U.S. study NEXICART-1 has demonstrated high complete response rates in relapsed/refractories AL Amyloidosis.XC-201 has been awarded Regenerative Medicine Advanced Therapy (RMAT) by the FDA, and Orphan Drug Designation (ODD) by the US FDA and in the EU by the EMA.

Latest news about Immix Biopharma, Inc.

Dec. 09	Immix Biopharma announces closing of upsized $100 million underwritten offering of common stock and pre-funded warrants	RE
Dec. 08	Immix Biopharma Prices $100 Million Offering	MT
Dec. 08	Immix Biopharma Prices $100 Million Offering	MT
Dec. 07	Immix Biopharma prices offering of 19.1 million shares at $5.10 per share	RE
Dec. 07	Immix Biopharma, Inc. Reports Positive Phase 2 NXC-201 Results, Advancing Toward BLA Submission as a Potentially First- and Best-In-Class Therapy for Relapsed/Refractory AL Amyloidosis	CI
Nov. 12	Immix Biopharma, Inc. Appoints Michael Grabow as Chief Commercial Officer	CI
Nov. 07	Immix Biopharma, Inc. Reports Earnings Results for the Third Quarter and Nine Months Ended September 30, 2025	CI
Sep. 18	Immix Biopharma says that 50% enrollment has already been surpassed in NEXICART-2	RE
Sep. 18	Immix Biopharma, Inc. Announces 50% Enrollment Milestone Surpassed in Its Ongoing Relapsed/Refractory AL Amyloidosis Clinical Trial, NEXICART-2	CI
Sep. 08	Immix Biopharma Gets Strategic Investment	MT
Sep. 08	Immix Biopharma announces strategic investment by Houston based Goose Capital, led by founding member Dr. Nancy T. Chang	RE
Sep. 08	Immix Biopharma, Inc. Appoints Nancy Chang, Ph.D. as A Member of the Board, Effective September 8, 2025	CI
Sep. 04	Immix Biopharma, Inc. announced that it has received $9.079982 million in funding	CI
Aug. 08	Immix Biopharma, Inc. Reports Earnings Results for the Second Quarter and Six Months Ended June 30, 2025	CI
Aug. 06	Immix Biopharma plans to partner-out other serious disease programs	RE
Aug. 06	Immix Biopharma, Inc. Announces Other Serious Diseases Strategy	CI
Jul. 11	Immix Biopharma Says NXC-201 Safety Profile Shows Absence of Neurotoxicity in Low-Volume Disease	MT
Jul. 11	Immix Biopharma Announces Class-Leading Safety Profile, Allowing Potential Future Indication Expansion	CI
Jun. 03	Immix Biopharma's NXC-201 Trial Meets Primary Endpoint in AL Amyloidosis	MT
May. 23	Immix Biopharma Further Expands U.S. Clinical Sites for Relapsed/Refractory AL Amyloidosis Trial Nexicart-2	CI
May. 23	Immix Biopharma Further Expands U.S. Clinical Sites for relapsed/refractory AL Amyloidosis Trial NEXICART-2	RE
May. 22	Immix Biopharma Announces Positive Results for NXC-201 at ASCO Oral Presentation, Enabling Pathway to Best-In-Class Therapy for Relapsed/Refractory AL Amyloidosis	CI
May. 08	Immix Biopharma, Inc. Reports Earnings Results for the First Quarter Ended March 31, 2025	CI
Mar. 25	Immix Biopharma, Inc. Reports Earnings Results for the Full Year Ended December 31, 2024	CI
Feb. 10	Immix Biopharma Says FDA Grants Regenerative Medicine Advanced Therapy Designation to NXC-201 Cell Therapy	MT

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Company Profile

Immix Biopharma, Inc. is a clinical-stage biopharmaceutical company. The Company is focused on the application of chimeric antigen receptor cell therapy (CAR- T) in light chain (AL) Amyloidosis and autoimmune disease. The Company's lead cell therapy asset is CAR-T NXC-201 for autoimmune disease, relapsed/refractory AL Amyloidosis, and relapsed/refractory multiple myeloma, which is being evaluated in its ongoing Phase Ib/IIa NEXICART-1 (NCT04720313) clinical trial. Its tissue specific therapeutic IMX-110 is in clinical trials as a monotherapy, and in combination with tislelizumab (BeiGene anti-PD-1 - IMMINENT-01 NCT05840835) for advanced solid tumors, such as relapsed/refractory colorectal cancer (CRC). IMX-110 in Phase Ib/IIa clinical trials, is a Tissue-Specific Therapeutic with TME Normalization, a technology that the Company is developing initially for mCRC and Soft Tissue Sarcoma (STS).

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