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Genprex wins FDA Fast Track designation for REQORSA with Keytruda for treating NSCLC

Genprex wins FDA Fast Track designation for REQORSA with Keytruda for treating NSCLC

Genprex Inc CEO Rodney Varner tells Proactive the FDA has granted Fast Track designation to the company’s lead drug candidate, REQORSA Immunogene Therapy, in combination with Merck & Co Inc (NYSE:MRK) (Merck & Co Inc (NYSE:MRK))’s Keytruda in patients with stage III or IV non-small cell lung cancer (NSCLC), where disease progressed after treatment with Keytruda.

The Austin, Texas-based clinical-stage gene therapy company said that in the first quarter of 2022, it plans to initiate its Acclaim-2 clinical trial, which is an open-label, multicenter Phase 1/2 clinical trial evaluating REQORSA in combination with Keytruda, for this patient population.

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