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Immix Biopharma Says Patients Dosed in AL Amyloidosis Trial Safety Run-in Successfully Complete Safety Evaluation
Express News | Immix Biopharma Inc: On Track for Next Program Update in Q1 2025
Immix Biopharma Accelerates Enrollment in U.S. AL Amyloidosis Trial of NXC-201 CAR-T
Independent Director of Immix Biopharma Picks Up 5.6% More Stock
Sector Update: Health Care Stocks Decline Late Afternoon
Immix Biopharma Announces Initial Data From First Four Patients In NEXICART-2 US Study; Says All Four Patients Treated With NXC-201 Normalized Disease Markers Within 30 Days Of Dosing, Of Which, Two Are Already Classified As Complete