Kestrel receives FDA Fast Track designation for KST-6051
The designation applies to the pan-KRAS inhibitor treatment for advanced solid tumors in ongoing Phase 1 trials. This facilitates expedited review and frequent FDA communication.
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Biotechnology company developing KRAS-targeted cancer therapies
kestreltherapeutics.comLast updated
In short: Kestrel received FDA Fast Track designation for its pan-KRAS inhibitor and entered a $1.45 billion strategic agreement with AbbVie.
The designation applies to the pan-KRAS inhibitor treatment for advanced solid tumors in ongoing Phase 1 trials. This facilitates expedited review and frequent FDA communication.
The company also announced a strategic warrant agreement with AbbVie for up to $1.45 billion, including an exclusive acquisition option.
The Phase 1 trial FALCON will enroll patients with advanced KRAS-mutant solid tumors.
He brings extensive experience to the role, strengthening the Clinical Development team's capabilities.
WATERTOWN, Mass., Sept. 15, 2026 (GLOBE NEWSWIRE) -- ("Kestrel" or the "Company"), a clinical-stage biotechnology company developing next-generation small-molecule inhibitors targeting mutant KRAS, today announced...
J&J-Sail and AbbVie-Kestrel put a spotlight on the option-to-acquire structure — rare even in a record M&A year — with biotech and pharma leaders weighing...
WATERTOWN, Mass., March 05, 2026 (GLOBE NEWSWIRE) -- Kestrel Therapeutics Inc. (“Kestrel” or the “Company”), a clinical stage biotechnology company developing next-generation small-molecule inhibitors ...
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