Key Performance
More- Earnings Score: N/A
- Momentum Score: 38
- True Yield: N/A
- Financial Health Score: N/A
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Latest Research & News
Cadrenal Therapeutics announced research findings demonstrating that its first-in-class 12-LOX inhibitor CAD-1005 can reduce inflammation associated with obesity and Type 2 diabetes. Preclinical studies showed CAD-1005 improved glycemic control, reduced pancreatic β-cell loss, and lowered inflammatory markers. The company believes CAD-1005 could complement existing GLP-1 obesity medications. CAD-1005 is currently in clinical development for Heparin-Induced Thrombocytopenia (HIT), with a Phase 2 trial showing reduced thrombotic events.
03/12/2026, 8:00 AM • GlobeNewswire
Cadrenal Therapeutics acquired VLX-1005, a novel small-molecule inhibitor targeting heparin-induced thrombocytopenia (HIT), from Veralox Therapeutics. The drug candidate has shown promising Phase 2 results and received Orphan Drug and Fast Track designations from the FDA.
12/11/2025, 8:05 AM • Benzinga
Kuick Research released a comprehensive study on the US Orphan Drug Market, projecting market opportunities exceeding $190 billion by 2030, with over 850 orphan drugs in clinical trials and 500 marketed orphan drugs, highlighting significant investment potential in rare disease therapeutics.
10/31/2025, 6:19 AM • Benzinga
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MoreInformation as of 08/21/2026
Company Profile
Cadrenal Therapeutics, Inc. operates as a late-stage biopharmaceutical company that develops novel therapies for life-threatening immune and thrombotic conditions. The company is developing Tecarfarin, an oral vitamin K antagonist that is in Phase 3 clinical trial designed to prevent heart attacks, strokes, and deaths due to blood clots in patients requiring chronic anticoagulation, such as patients with left ventricular assist devices, end-stage kidney disease, and atrial fibrillation; CAD-1005, a first-in-class 12-LOX inhibitor for the treatment of heparin-induced thrombocytopenia, a deadly immune-mediated thrombotic disorder that has completed Phase 2 clinical trial; and Frunexian, a parenteral clinical-stage factor XIa inhibitor designed for use in acute hospital settings that has completed Phase 1 clinical trial. It has a collaboration agreement with Abbott Global Enterprises Limited to evaluate the efficacy and safety of Tecarfarin in patients with a left-ventricular assist device. The company was incorporated in 2022 and is headquartered in Ponte Vedra, Florida.