Inovio Pharmaceuticals 2025 Q3 Earnings Narrowed Loss per Share Amid Widening Net Loss

Generated by AI AgentDaily EarningsReviewed byAInvest News Editorial Team
Tuesday, Nov 11, 2025 1:47 am ET1min read
Aime RobotAime Summary

- Inovio's Q3 2025 earnings beat estimates with a $0.87 loss per share vs. $0.51 expected, though net losses widened despite cost cuts.

- The company extended its cash runway to Q2 2026 and submitted its first BLA for INO-3107, targeting RRP market leadership with improved tolerability and reduced surgical burden.

- A stock offering and regulatory milestones highlight strategic focus on financial stability and product launch readiness ahead of potential 2026 FDA approval.

Inovio Pharmaceuticals (INO) reported Q3 2025 earnings that beat Wall Street expectations, with a loss of $0.87 per share compared to the estimated $0.51 loss. The company maintained its cash runway through Q2 2026, , driven by non-cash warrant liabilities. Analysts remain optimistic, , reflecting confidence in its pipeline and cost discipline.

Revenue

.

Earnings/Net Income

. Meanwhile, , . While the EPS showed a 2.2% improvement, the widened net loss highlights ongoing financial challenges despite cost reductions.

Post-Earnings Price Action Review

Historical data suggests a favorable post-earnings strategy for

, with a 17.5% cumulative return over three years when holding for 30 days after a flat quarter-over-quarter revenue report. This translates to an average annual return of approximately 5.8%, indicating a viable medium-term approach despite modest gains driven by market and sector dynamics.

CEO Commentary

, CEO, highlighted completing the rolling BLA submission for INO-3107 as a key 2025 milestone, positioning it as Inovio’s first BLA and a critical step toward addressing the RRP market. She emphasized the product’s differentiators—superior tolerability, reduced , and a patient-centric regimen—as strategic priorities to secure market share despite being a second entrant. Strategic focus remains on commercial readiness, including partnerships and launch planning, alongside advancing next-gen DNA platforms (DMAb/DPROT). Leadership expressed optimism, citing clinical data showing 50%-100% surgery reduction in trials and confidence in INO-3107’s potential to become the “product of choice” for RRP patients.

Guidance

Inovio expects FDA BLA acceptance by year-end 2025, with a potential PDUFA date in mid-2026 under priority review; a Type D meeting is planned to finalize confirmatory trial design. Financially, Q3 2025 net loss was $45.5M (EPS -$0.87), with operating expenses down 22% YoY to $21.2M. Cash balances stood at $50.8M, projected to last through Q2 2026, . , despite ’ first-mover advantage.

Additional News

Inovio announced a common stock offering, granting a 30-day option to purchase additional shares, aiming to bolster its cash reserves. The company also completed its rolling BLA submission for INO-3107, targeting FDA acceptance by year-end 2025, with a potential mid-2026 launch. Additionally, , reflecting market skepticism about capital-raising activities. These developments underscore Inovio's strategic focus on regulatory milestones and financial stability ahead of its key product launch.

Comments



Add a public comment...
No comments

No comments yet