Immix Biopharma Says Patients Dosed in AL Amyloidosis Trial Safety Run-in Successfully Complete Safety Evaluation

MT Newswires Live
01-07

Immix Biopharma (IMMX) said Tuesday six patients dosed in a phase 1b safety run-in segment of a trial of its experimental NXC-201 treatment of relapsed or refractory AL Amyloidosis successfully completed the trial's safety evaluation.

The safety run-in segment dosed three patients at 150 million CAR-T cells and three patients at 450 million CAR-T cells.

Immix said enrollment can now advance across US study sites at a dose of 450 million CAR-T cells.

AL Amyloidosis is a life-threatening disorder of plasma cells in the bone marrow.

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