Immix Biopharma announced that the European Commission has granted orphan drug designation to NXC-201 for the treatment of multiple myeloma.
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Read More on IMMX:
- Immix Biopharma on Track to Dose NXC-201 Patients in United States
- Immix Biopharma says ‘on track’ to dose NXC-201 patients in U.S.
- 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)
- Immix Biopharma Announces Major Comprehensive Cancer Center as Lead Site for NXC-201 AL Amyloidosis Clinical Trial
- Immix announces Memorial Sloan Kettering as lead site for NXC-201 trial
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