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Immix Biopharma Announces Positive NXC-201 Relapsed/Refractory AL Amyloidosis Clinical Data in ASGCT 2024 Late Breaking Oral Presentation

Immix Biopharma Announces Positive NXC-201 Relapsed/Refractory AL Amyloidosis Clinical Data in ASGCT 2024 Late Breaking Oral Presentation
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NXC-201 Receives Orphan Drug Designation in European Union for Multiple Myeloma

The CAR T-cell therapy NXC-201 has received orphan drug designation by the European Commission for patients with multiple myeloma. ....

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Immix Biopharma Awarded European Union Orphan Drug Designation for NXC-201 in Multiple Myeloma

European Orphan Drug Designation qualifies NXC-201 for: 10 years of market exclusivity once authorized in the EUAccess to the EU centralized authorization procedureReduced fees for: EU protocol. ....

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Immix Biopharma on Track to Dose NXC-201 Patients in United States

Scheduling U.S. site initiation visits April and May 2024On track to dose relapsed/refractory AL Amyloidosis patients with CAR-T NXC-201 at New York City lead site and other leading U.S.. ....

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Nexcella, an Immix Biopharma Subsidiary, on Track to Dose NXC-201 Patients in United States

Nexcella, an Immix Biopharma Subsidiary, on Track to Dose NXC-201 Patients in United States
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