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Immix Biopharma expands U.S. clinical sites for NEXICART-2 trial
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Immix Biopharma receives FDA RMAT designation for NCX-201 in r/r AL Amyloidosis
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Immix Biopharma accelerates enrollment in U.S. AL amyloidosis trial of NXC-201
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Immix Biopharma announces data from four patients in NEXICART-2 U.S. trial
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Immix Biopharma announces publication of NXC-201 clinical results
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Immix Biopharma reports 75% CRR for NXC-201 in r/r AL amyloidosis patients
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Immix Biopharma: Ex-US study of NXC-201 produced 92% ORR in r/r AL Amyloidosis
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Immix Biopharma announces three more sites for NEXICART-2 trial
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Immix Biopharma awarded $8M CLIN2 grant
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Immix Biopharma doses first patient in U.S. AL amyloidosis trial with NXC-201
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Immix Biopharma Shareholders Back Growth and Governance Changes
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Immix Biopharma announces NXC-201 relapsed/refractory AL Amyloidosis data
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Immix Biopharma management to meet with B. Riley
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Immix Biopharma: EC grants orphan drug designation to NXC-201
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Immix Biopharma says ‘on track’ to dose NXC-201 patients in U.S.
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Immix announces Memorial Sloan Kettering as lead site for NXC-201 trial
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Immix Biopharma: EC grants orphan drug designation to NXC-201
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