Regeneron investors face Sept. 14 lead-plaintiff deadline after melanoma trial failure

  • Regeneron investors can seek lead-plaintiff appointment in a securities class action.
  • Sept. 14, 2026, is the deadline for investors to seek lead-plaintiff status.
  • Regeneron reported the Phase III study missed its primary endpoint on May 15, 2026.

Regeneron investors who purchased or acquired the company’s common stock from Aug. 1, 2025, through May 15, 2026, have until Sept. 14, 2026, to seek appointment as lead plaintiff in a securities class action filed in the U.S. District Court for the Southern District of New York. The case, Cheatham v. Regeneron Pharmaceuticals, Inc., No. 26-cv-06026, names Regeneron and certain top executives and alleges violations of the Securities Exchange Act of 1934. The complaint centers on disclosures about the Phase III Fianlimab-Libtayo study in melanoma, which failed to achieve statistical significance for its primary endpoint of progression-free survival. Regeneron disclosed a study alteration on April 29, 2026, and reported the failed trial after market close on May 15; the complaint says the stock fell more than 6% after the April disclosure and nearly 10% after the May announcement, while an earlier investor announcement attributed an $11 billion market-capitalization loss to the failure. Robbins Geller Rudman & Dowd LLP is soliciting investors seeking lead-plaintiff status, while Hagens Berman has separately announced an investigation and earlier litigation-related claims concerning the disclosures.

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