United States — Food and Drug Administration & Lewis Kahn
6 shared events · Importance 3 · Last updated Apr 27, 2026
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Regulatory
United States — Food and Drug Administration: The FDA published briefing documents critical of Capricor's statistical analysis plan and raised concerns about the benefit-risk profile of Deramiocel. This regulatory action triggered the stock drop and the subsequent lawsuit, and it may influence the advisory committee's decision on the BLA.
Lewis Kahn: Lewis Kahn is the Managing Partner at Kahn Swick & Foti and is the contact person for investors in the class action lawsuit. He plays a key role in soliciting investors and managing the case.
Aug 18, 2026 · 6 articles
Regulatory
United States — Food and Drug Administration: The United States — Food and Drug Administration issued a warning letter to ImmunityBio regarding misleading efficacy claims made by Patrick Soon-Shiong about Anktiva, which triggered the stock price drop and subsequent lawsuits.
Lewis Kahn: Lewis Kahn is the Managing Partner of Kahn Swick & Foti, LLC, and is involved in reminding investors about the class action lawsuit.
Apr 02, 2026 · 132 articles
Regulatory
United States — Food and Drug Administration: Regulator whose briefing documents and advisory committee vote triggered the stock collapse and legal actions.
Lewis Kahn: Managing partner at Kahn Swick & Foti involved in the lawsuit.
Jul 27, 2026 · 293 articles
Regulatory
Lewis Kahn: Lewis Kahn is the Managing Partner at Kahn Swick & Foti, involved in the class action lawsuit against UniQure.
Apr 01, 2026 · 25 articles
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