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Immix Biopharma's NXC-201 Trial Meets Primary Endpoint in AL Amyloidosis
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Immix Biopharma's NXC-201 Trial Meets Primary Endpoint in AL Amyloidosis
Jun 3, 2025 12:52 PM

03:30 PM EDT, 06/03/2025 (MT Newswires) -- Immix Biopharma ( IMMX ) said the US multisite clinical trial evaluating its NXC-201 cell therapy in relapsed or refractory AL Amyloidosis achieved its primary endpoint of complete response.

NXC-201 treatment resulted in a 70% complete response rate, and all of the patients in the trial had baseline relapsed or refractory AL Amyloidosis organ involvement, the company said Tuesday in a statement.

The company plans to submit a biologics license application for approval from the Food and Drug Administration.

The interim results of the Phase 1/2 study were presented at a clinical oncology conference in Chicago.

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