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Immix Biopharma, Inc : Immix Biopharma Announces FDA Approval of IND Application for CAR-T NXC-201, Enabling U S Patient Dosing

Immix Biopharma, Inc : Immix Biopharma Announces FDA Approval of IND Application for CAR-T NXC-201, Enabling U S Patient Dosing
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Immix Biopharma Announces FDA Approval of IND Application for CAR-T NXC-201, Enabling U S Patient Dosing

Immix Biopharma Presents NXC-201 Data at 65th American Society of Hematology (ASH) Annual Meeting in 9 Relapsed/Refractory AL Amyloidosis Patients

100% overall response rate observed in relapsed/refractory AL Amyloidosis patients with median 6 lines of prior therapyUpdated results will be communicated at the presentation time December 10,.

Immix Biopharma Presents NXC-201 Data at 65th American Society of Hematology (ASH) Annual Meeting in 63 Relapsed/Refractory Multiple Myeloma Patients

Immix Biopharma Presents NXC-201 Data at 65th American Society of Hematology (ASH) Annual Meeting in 63 Relapsed/Refractory Multiple Myeloma Patients
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Immix Biopharma (IMMX) to present additional NXC-201 clinical data at ASH

Immix Biopharma (IMMX) to present additional NXC-201 clinical data at ASH
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