Sarepta Therapeutics Faces Turbulent Times Amid Deaths and Lawsuits

Sarepta Therapeutics Encounters Severe Stock Drop Following Patient Deaths

Investors in Sarepta Therapeutics, Inc. (NASDAQ: SRPT) witnessed a staggering drop of 36% in share prices, exacerbated by troubling news surrounding patient fatalities linked to the company's experimental gene therapy treatments. The values plummeted after reports emerged regarding the death of a third patient, resulting in a close of $7.89 down on July 18, 2025.

Overview of Legal Actions and Investigations

In this challenging landscape, a securities class action lawsuit named Dolgicer v. Sarepta Therapeutics, Inc. has emerged, seeking to represent investors who acquired Sarepta's securities during a specific period. The class period for this litigation spans from June 22, 2023, to June 24, 2025. Notably, national shareholder rights firm Hagens Berman is actively investigating the legal claims involved in the case.

Understanding the Concerns Around ELEVIDYS

The lawsuit scrutinizes the company's disclosures about ELEVIDYS, a gene therapy aimed at addressing Duchenne muscular dystrophy. Claimants allege that Sarepta led investors to believe that ELEVIDYS was safe, downplaying the risks associated with its application and potential for broader approval.

Safety Risks Alleged in Lawsuit

Serious accusations have surfaced related to the safety of ELEVIDYS, asserting that significant risks to patients were not adequately communicated by Sarepta. Investors argue that the clinical trial protocols were insufficient in detecting adverse effects, raising the alarm on the severity of the incidents resulting in death.

Impact of Recent Developments on Shareholder Trust

The troubling updates began with an initial safety alert from Sarepta, revealing one patient’s death during the trial phases. Additionally, further developments disclosed two other fatalities linked to the treatment of ELEVIDYS. Each instance triggered alarming sentiments within the investor community, leading to abrupt stock price declines.

Regulatory Scrutiny Intensifies

Amidst these incidents, the FDA has stepped in to review the situation surrounding Sarepta's investigational gene therapies. Following the adverse events, the FDA issued safety communications detailing investigations into these occurrences, amplifying concerns regarding the future of ELEVIDYS.

Investor Reactions and Consequences

As uncertainty looms, investor sentiment has turned cautious. The stock price drop has resulted in H.C. Wainwright drastically revising its price target for Sarepta. Reed Kathrein, a prominent partner at Hagens Berman, expressed ongoing concerns about the potential misinformation affecting investor decisions associated with the gene therapy's future.

Company's Contact Information

For those impacted or possessing information that may aid the ongoing investigation, Hagens Berman encourages affected investors to come forward and share their experiences. Contact the firm at 844-916-0895 or via email at SRPT@hbsslaw.com.

Frequently Asked Questions

What led to Sarepta Therapeutics' stock drop?

The stock dropped following reports of patient deaths associated with their gene therapy treatments, specifically ELEVIDYS.

What is the ongoing lawsuit against Sarepta about?

The lawsuit concerns allegations that Sarepta misrepresented the safety of ELEVIDYS and failed to disclose significant risks to investors.

How are regulatory bodies responding to the deaths?

The FDA has launched investigations into the incidents, and Sarepta has been subject to scrutiny regarding its investigational therapies.

Who can participate in the investors' class action lawsuit?

Investors who purchased or acquired Sarepta securities between June 22, 2023, and June 24, 2025, may qualify to be part of the class action.

Where can I find more information about Sarepta Therapeutics' legal situation?

For further details, Hagens Berman's website and legal publications provide comprehensive insights into Sarepta's circumstances.

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