Cadrenal Therapeutics (NASDAQ: CVKD) is developing tecarfarin, a late-stage novel oral and reversible anticoagulant (blood thinner), to prevent heart attacks, strokes, and deaths due to blood clots in patients with certain rare medical conditions who require chronic anticoagulation. Tecarfarin has orphan drug and Fast Track designations for the prevention of systemic thromboembolism (blood clots) of cardiac origin in patients with end-stage kidney disease (“ESKD”) with atrial fibrillation (“AFib”), and also is being evaluated for the treatment of heart disease in patients with implanted medical devices such as left ventricular assist devices (“LVADs”), as well as in patients with antiphospholipid syndrome (“APS”). Tecarfarin is specifically designed to leverage a different metabolic pathway than the oldest and most commonly prescribed Vitamin K Antagonist (warfarin) used in the prevention of thrombosis. Tecarfarin has been evaluated in eleven (11) human clinical trials and more than 1,000 individuals. In Phase 1, Phase 2, and Phase 2/3 clinical trials, tecarfarin has generally been well-tolerated in both healthy adult subjects and patients with chronic kidney disease. For more information, visit the company’s website at www.cadrenal.com.
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