Immix Biopharma Awarded European Union Orphan Drug Designation for NXC-201 in AL Amyloidosis
Immix Biopharma, Inc. (IMMX)
Company Research
Source: GlobeNewswire
European Orphan Drug Designation (“ODD”) qualifies NXC-201 for: 10 years of market exclusivity once authorized in the EUAccess to the EU centralized authorization procedureReduced fees for EU protocol assistance, marketing authorization applications, inspections before authorization, applications for changes to marketing authorizations made after approval, and reduced annual fees U.S. observed prevalence of relapsed/refractory AL Amyloidosis is growing 12% per year according to Staron, et al Blood Cancer Journal, estimated to reach 29,712 patients in 2023 Los Angeles, Feb. 07, 2024 (GLOBE NEWSWIRE) -- Immix Biopharma, Inc. (“Immix Biopharma”, “Company”, “We” or “Us”, Nasdaq:IMMX), a clinical-stage biopharmaceutical company trailblazing cell therapies in autoimmune disease, today announced that the European Commission (EC) has granted orphan drug designation to NXC-201 for the treatment of AL Amyloidosis. “European Union orphan drug designation for NXC-201 represents an imp
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News
- Immix Biopharma Awarded European Union Orphan Drug Designation for NXC-201 in Multiple Myeloma [Yahoo! Finance]Yahoo! Finance
- Immix Biopharma Awarded European Union Orphan Drug Designation for NXC-201 in Multiple MyelomaGlobeNewswire
- Nexcella, an Immix Biopharma Subsidiary, on Track to Dose NXC-201 Patients in United States [Yahoo! Finance]Yahoo! Finance
- Immix Biopharma on Track to Dose NXC-201 Patients in United StatesGlobeNewswire
- Immix Biopharma Announces Late-Breaking NXC-201 Clinical Data Abstract Accepted for Oral Presentation at the 27th Annual Meeting of the American Society of Gene and Cell Therapy (ASGCT)GlobeNewswire
IMMX
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- 4/30/24 - Form ARS
- 4/29/24 - Form DEF
- 3/29/24 - Form 10-K
- IMMX's page on the SEC website