On track to submit Biologics License Application (BLA) for INO-3107 in 2H25, with the goal of file acceptance by year end Completed design verification (DV) testing of CELLECTRA® 5PSP device required for BLA submission and requested rolling submission from US Food and Drug Administration (FDA) Continuing to advance commercial preparations for potential launch of INO-3107 in 2026 if approved by FDA PLYMOUTH MEETING, Pa. ,... Read More