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Inovio Pharmaceuticals Reports Q2 2025 Financial Progress

Inovio Pharmaceuticals Reports Q2 2025 Financial Progress

Inovio Pharmaceuticals ( (INO) ) has released its Q2 earnings. Here is a breakdown of the information Inovio Pharmaceuticals presented to its investors.

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Inovio Pharmaceuticals is a biotechnology company specializing in the development and commercialization of DNA medicines aimed at treating HPV-related diseases, cancer, and infectious diseases. The company is recognized for its innovative approach using DNA plasmids and proprietary delivery devices.

Inovio Pharmaceuticals has reported its financial results for the second quarter of 2025, highlighting significant progress in its pipeline, particularly with the INO-3107 treatment for Recurrent Respiratory Papillomatosis (RRP). The company is on track to submit a Biologics License Application (BLA) for INO-3107 in the latter half of 2025, aiming for FDA acceptance by year-end.

Key financial metrics indicate a reduction in operating expenses, with research and development costs decreasing from $23.1 million in 2024 to $14.5 million in 2025. General and administrative expenses also saw a decline, contributing to a reduced net loss of $23.5 million compared to $32.2 million in the previous year. The company has strengthened its financial position with a $22.5 million public offering.

Inovio’s strategic advancements include the completion of design verification testing for its CELLECTRA 5PSP device, essential for the BLA submission. The company is preparing for a potential commercial launch of INO-3107 in 2026, contingent on FDA approval. Additionally, Inovio is exploring next-generation DNA medicine technologies, presenting promising data at various upcoming scientific conferences.

Looking ahead, Inovio remains committed to advancing its pipeline and optimizing its resources. The management anticipates that the current cash reserves, bolstered by recent funding, will support operations into the second quarter of 2026, as they continue to focus on achieving regulatory milestones and potential market entry for their innovative treatments.

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