Faruqi & Faruqi Investigates Potential Claims Against Inovio
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Feb 25 2026
0mins
Should l Buy INO?
Source: Globenewswire
- Legal Investigation Launched: Faruq & Faruqi LLP is investigating potential claims against Inovio Pharmaceuticals, specifically targeting investors who purchased securities between October 10, 2023, and December 26, 2025, aiming to provide legal support for affected investors.
- Overview of Allegations: The complaint alleges that Inovio and its executives violated federal securities laws, particularly citing deficiencies in the manufacturing of the CELLECTRA device, which hindered the timely submission of the INO-3107 Biologics License Application (BLA) and negatively impacted the company's market outlook.
- FDA Response and Stock Price Impact: On December 29, 2025, the FDA accepted Inovio's BLA but noted that the company failed to provide adequate information for accelerated approval, resulting in a 24.45% drop in Inovio's stock price to $1.73 per share, reflecting market concerns about the company's future prospects.
- Investor Action Call: Faruq & Faruqi encourages anyone with information, including former employees and shareholders, to contact the firm, emphasizing investors' rights and potential recovery opportunities in the class action lawsuit.
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Analyst Views on INO
Wall Street analysts forecast INO stock price to rise
3 Analyst Rating
2 Buy
1 Hold
0 Sell
Moderate Buy
Current: 1.730
Low
3.00
Averages
7.33
High
13.00
Current: 1.730
Low
3.00
Averages
7.33
High
13.00
About INO
Inovio Pharmaceuticals, Inc. is a biotechnology company focused on developing and commercializing deoxyribonucleic acid (DNA) medicines to help treat and protect people from human papillomavirus (HPV)-related diseases, cancer, and infectious diseases. Its proprietary investigational CELLECTRA devices are designed to deliver the plasmids into the body’s cells for optimal effect, without the use of chemical adjuvants, lipid nanoparticles or viral vectors. Its lead candidate is INO-3107 for the treatment of recurrent respiratory papillomatosis (RRP), a chronic, rare and debilitating disease caused by HPV-6 and HPV-11. Its DNA medicines in the pipeline include INO-3112 for the Treatment of HPV-related Oropharyngeal Squamous Cell Carcinoma, VGX-3100 for the Treatment of HPV-related Cervical HSIL, VGX-3100 for the Treatment of Anal or Perianal HSIL, INO-5401 for the Treatment of Glioblastoma Multiforme (GBM), and INO-5401 for the Prevention of Cancer for People with BRCA1/2 Mutation.
About the author

Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
- Legal Investigation Launched: Faruq & Faruqi, LLP is investigating potential claims against Inovio Pharmaceuticals, particularly for investors who purchased or acquired securities between October 10, 2023, and December 26, 2025, aiming to protect investor rights.
- Investor Contact Information: Securities Litigation Partner Josh Wilson encourages affected investors to contact him directly at 877-247-4292 or 212-983-9330 (Ext. 1310) to discuss their legal options, ensuring timely legal support for investors.
- Class Action Deadline: Investors should note that the deadline to seek lead plaintiff status in the federal securities class action against Inovio is April 7, 2026, a critical date that may affect their rights to claim.
- Law Firm Background: Faruq & Faruqi, LLP is a leading national securities law firm focused on protecting investor rights through investigations and litigation, demonstrating its expertise and influence in the field of securities law.
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- Inovio Pharmaceuticals Issues: Inovio Pharmaceuticals, Inc. is facing a class action lawsuit for the period from October 10, 2023, to December 26, 2025, due to deficiencies in manufacturing its CELLECTRA device, which is expected to hinder its ability to submit the INO-3107 BLA to the FDA by the second half of 2024, affecting its regulatory and commercial prospects.
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- Class Action Filed: Pomerantz LLP has initiated a class action lawsuit against Inovio Pharmaceuticals and certain executives in the Eastern District of Pennsylvania, representing investors who purchased Inovio securities between October 2023 and December 2025, seeking damages for violations of federal securities laws.
- False Statements Uncovered: The lawsuit alleges that Inovio made materially false and misleading statements throughout the class period, failing to disclose manufacturing deficiencies in its CELLECTRA device, which delayed the submission of the INO-3107 BLA to the FDA until mid-2025, undermining investor confidence.
- Stock Price Volatility: Following the announcement of the delayed BLA submission on August 9, 2024, Inovio's stock price fell by 3.1% to close at $8.44 per share; subsequently, on December 29, 2025, the stock plummeted by 24.45% to $1.73 per share after the FDA accepted the BLA for standard review instead of accelerated review.
- Investor Rights at Stake: The lawsuit highlights significant economic losses suffered by investors due to Inovio's misleading statements, with Pomerantz LLP, a leading firm in securities class action litigation, committed to advocating for the rights of affected investors and seeking compensation.
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- Lawsuit Notice Issued: The Gross Law Firm has issued a notice to shareholders of Inovio Pharmaceuticals, encouraging those who purchased shares between October 10, 2023, and December 26, 2025, to contact the firm regarding potential lead plaintiff status.
- Allegations Overview: The complaint alleges that Inovio made materially false or misleading statements during the class period, particularly regarding deficiencies in the manufacturing of its CELLECTRA device, which jeopardizes the timeline for submitting INO-3107 to the FDA.
- Critical Deadline: Shareholders must register by April 7, 2026, to participate in the class action, emphasizing the urgency of the legal process and the potential impact on their rights to claim damages.
- No Cost Participation: Once registered, shareholders will receive portfolio monitoring updates throughout the case lifecycle, and participation incurs no costs, highlighting the accessibility and transparency of legal services offered by the firm.
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- Class Action Reminder: The Schall Law Firm alerts investors of a class action lawsuit against Inovio Pharmaceuticals for violations of §§10(b) and 20(a) of the Securities Exchange Act, concerning securities purchased between October 10, 2023, and December 26, 2025, with a deadline to contact the firm by April 7, 2026.
- False Statements Allegation: The complaint alleges that Inovio had manufacturing deficiencies with its CELLECTRA device and is unlikely to file the INO-3107 BLA by the second half of 2024, rendering the company's public statements throughout the class period false and misleading.
- Investor Losses: As the market learned the truth about Inovio, investors suffered damages, indicating the company's failure to provide sufficient evidence for FDA priority review or accelerated approval, which further eroded investor confidence.
- Legal Consultation Opportunity: The Schall Law Firm offers free consultations and encourages affected shareholders to discuss their rights, demonstrating the firm's commitment to protecting investor interests while reminding investors that they are not represented until the class action is certified.
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- Inovio's Regulatory Challenges: Inovio Pharmaceuticals, Inc. (NASDAQ:INO) is facing a class action lawsuit for the period from October 10, 2023, to December 26, 2025, alleging that the company did not disclose deficiencies in the manufacturing of its CELLECTRA device, which jeopardizes the prospects of its Biologics License Application, leading to a decline in investor confidence.
- FDA Review Impact: Although Inovio's Biologics License Application was accepted by the FDA on December 29, 2025, the company failed to provide adequate information for accelerated approval, resulting in a 24.45% drop in stock price, reflecting market concerns about its future commercial prospects.
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