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Cadrenal Therapeutics Announces End-of-Phase 2 Meeting with the FDA and Pivotal Phase 3 Registration Path for CAD-1005 in Heparin-Induced Thrombocytopenia (HIT)

FDA provided critical guidance for the advancement of CAD-1005 to pivotal Phase 3 in HIT Phase 2 data showed a greater than 25% absolute reduction in thrombotic events when CAD-1005 was added to standard anticoagulant therapy PONTE VEDRA, Fla., April 30, 2026 (GLOBE NEWSWIRE) -- Cadrenal Therapeutics, Inc. (Nasdaq: CVKD), a biopharmaceutical company developing innovative treatments for life-threatening immune and thrombotic conditions, today announced a major regulatory milestone after successfu

articleCadrenal Therapeutics, Inc.April 30, 20266/company/cadrenal-therapeutics-inc-common-stock/news/cadrenal-therapeutics-announces-end-of-phase-2-meeting-with-the-fda-and-pivotal-phase-3-registration-path-for-cad-1005-in-heparin-induced-thrombocytopenia-hit
Cadrenal Therapeutics Announces End-of-Phase 2 Meeting with the FDA and Pivotal Phase 3 Registration Path for CAD-1005 in Heparin-Induced Thrombocytopenia (HIT)

About this update from Cadrenal Therapeutics, Inc.

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More updates from Cadrenal Therapeutics, Inc.

pivotal trialanticoagulant therapythrombotic eventsPhase 3 studyCadrenal Therapeutics, IncpatientsThe CompanyFood and Drug AdministrationHeparin-Induced Thrombocytopenia