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Faruqi Faruqi Investigates PepGen Over Securities Violations Amid FDA Concerns

WHAT'S THE STORY?

What's Happening?

Faruqi & Faruqi, LLP, a national securities law firm, is investigating potential claims against PepGen Inc. following allegations of securities law violations. The firm is encouraging investors who suffered losses between March 7, 2024, and March 3, 2025, to consider their legal options. The investigation centers on claims that PepGen and its executives made false or misleading statements regarding the effectiveness and safety of PGN-EDO51, a drug involved in the CONNECT2 clinical trial. The FDA issued a clinical hold notice for the trial, citing concerns about patient risks and study deficiencies. This led to a significant drop in PepGen's stock price. The firm is seeking a lead plaintiff for a class action lawsuit, with a deadline set for August 11, 2025.
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Why It's Important?

The investigation into PepGen's conduct is significant as it highlights the potential impact of corporate misrepresentation on investors and the pharmaceutical industry. If the allegations are proven, it could lead to substantial financial repercussions for PepGen and affect investor confidence. The case underscores the importance of transparency and compliance with regulatory standards in clinical trials, which are crucial for public safety and investor trust. The outcome of this investigation could influence how pharmaceutical companies communicate trial results and manage investor relations, potentially leading to stricter regulatory oversight.

What's Next?

Investors affected by PepGen's alleged misconduct have until August 11, 2025, to seek the role of lead plaintiff in the class action lawsuit. The legal proceedings will likely involve detailed scrutiny of PepGen's communications and trial management practices. The firm is also encouraging whistleblowers and individuals with relevant information to come forward. The case may prompt further regulatory reviews and adjustments in how clinical trials are conducted and reported, impacting future pharmaceutical industry practices.

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