$INO

INOVIO PHARMACEUTICALS, INC.

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Inovio Pharmaceuticals Shareholders Back Board as INO-3107 FDA Review Advances

Inovio Pharmaceuticals said the FDA completed a standard mid-cycle review of its BLA for INO-3107 for recurrent respiratory papillomatosis, with “no new significant issues,” and scheduled the late-cycle review for Q3. The company expects an informal meeting on an Accelerated Approval eligibility question. Inovio reported $37.7M cash at Q1 2026, reduced 2025 operating spend 23%, and expects runway into Q1 2027.

Investigation Alert: Investors who hold shares of Inovio

An investigation has been launched by the Shareholders Foundation on behalf of long-term investors in Inovio Pharmaceuticals, Inc. (NASDAQ: INO) regarding potential breaches of fiduciary duties by certain directors. This follows a lawsuit alleging securities law violations after INO's share price plummeted due to delays in FDA submissions for its lead product candidate, INO-3107, and issues with its CELLECTRA device. The investigation concerns whether Inovio directors are liable for false or misleading statements regarding manufacturing, submission timelines, and regulatory prospects.

INOVIO (NASDAQ: INO) details Q1 loss and INO-3107 accelerated FDA review

INOVIO reported a net loss of $19.7 million for Q1 2026, consistent with the previous year, while significantly reducing operating expenses. The company's lead candidate, INO-3107, is under accelerated FDA review for recurrent respiratory papillomatosis, with a target PDUFA date of October 30, 2026, and INOVIO is preparing for a potential 2026 commercial launch. INOVIO projects its current cash, supplemented by recent equity offering proceeds, will fund operations into Q1 2027, beyond the FDA's decision date for INO-3107.

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