[Asia Economy Reporter Minji Lee] Olix announced on the 29th that it has received approval from the U.S. Food and Drug Administration (FDA) for a Phase 2a clinical trial plan to evaluate the efficacy of OLX100 as an adjuvant therapy to suppress recurrence after scar reconstruction surgery.



The target condition is hypertrophic scars. The company stated, "We will verify the efficacy and safety of OLX100 and proceed with the next phase of clinical trials based on this," adding, "This confirms the potential for developing a new treatment in the hypertrophic scar market, where no FDA-approved prescription drugs currently exist."


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