Keenova FDA Tuesday, April 29, 1952 +0.20 Positive

FDA Approves ACTHAR — Keenova ARD LLC

Keenova ARD LLC has announced FDA approval for Repository Corticotropin Injection (Acthar), a long-established therapy originally approved in 1952, expanding critical options for treating certain autoimmune disorders and severe infant spasms. This landmark approval ensures continued market availability of the biologic, providing a vital lifeline for patients historically reliant on this specific injectable product.

View original filing at SEC.gov →
AI-generated summary for informational purposes only. Always verify against the original filing. Not investment advice. BriefTape is not a registered investment adviser.

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