Immix gets FDA’s green light to expand trial for cancer combination therapy

Immix Biopharma, said Tuesday it got a letter from the FDA authorizing it to expand its phase 1b/2a clinical trial of IMX-110 to the United States under an IND.

Immix said that, to-date, interim readouts from the phase 1b/2a trial in Australia are 100% CBR / DCR for all patients who completed the 5th cohort and at least 2 cycles, as scheduled – with the longest duration of response being 8-months of stable disease. No treatment-related serious adverse events have been observed to-date in any cohorts and dose escalation is continuing.

Immix’ Interim Medical Director and CEO Ilya Rachman, MD, PhD said: “We were quite surprised and incredibly happy to see real clinical benefits of the drug at such an early stage in the trial. We are excited to explore the extent of this drug’s potential as we progress with dose escalation and approach the expected optimal therapeutic dose of the drug.”

At present, Immix is finalizing selection of US clinical sites that will participate in this Phase 1b/2a multinational trial for advanced solid tumors, it was stated in the press release.