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Rapt Therapeutics: FDA clears IND application for Phase 2b trial of RPT904

Rapt Therapeutics (RAPT) announced that the U.S. FDA has cleared Rapt’s Investigational New Drug Application to proceed to a Phase 2b clinical trial of RPT904 for the treatment of patients with food allergy. The planned Phase 2b trial in food allergy is a randomized double-blind placebo-controlled study designed to evaluate the safety and efficacy of RPT904 dosed every 8 weeks and every 12 weeks.

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