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Cadrenal Therapeutics (CVKD) investor relations material

Cadrenal Therapeutics Registration Filing summary

Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
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Registration Filing summary29 Dec, 2025

Company overview and business model

  • Focuses on developing novel products for acute and chronic anticoagulation management in rare and high-risk patient populations, with three clinical-stage assets: VLX-1005 (12-LOX inhibitor for HIT), tecarfarin (oral VKA for chronic use), and frunexian (IV Factor XIa inhibitor for acute care settings).

  • Recently acquired all rights and assets related to VLX-1005 and related compounds from Veralox Therapeutics.

  • Incorporated in Delaware in January 2022, with principal offices in Ponte Vedra, Florida.

Financial performance and metrics

  • Net tangible book value as of September 30, 2025, was $2.7 million ($1.33 per share); pro forma net tangible book value after recent offerings and warrant exercises would be $10.1 million ($3.64 per share).

  • Gross proceeds from the December 2025 offering were approximately $2.2 million.

Use of proceeds and capital allocation

  • Will not receive proceeds from the resale of shares by selling stockholders; proceeds from any cash exercise of warrants will be used for working capital and general corporate purposes.

  • Management retains broad discretion over allocation of net proceeds from warrant exercises.

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Q4 202512 Mar, 2026
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Q4 202512 Mar, 2026

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Frequently asked questions

Cadrenal Therapeutics, Inc. is a biopharmaceutical company focused on the development of tecarfarin, an advanced oral anticoagulant. Tecarfarin is designed to prevent heart attacks, strokes, and deaths caused by blood clots, particularly in patients with rare cardiovascular conditions that require long-term anticoagulation therapy. These conditions include end-stage kidney disease (ESKD), atrial fibrillation, and complications related to left ventricular assist devices (LVADs). The company aims to address the limitations of existing anticoagulants like warfarin, offering a more stable and reliable treatment option through an alternative metabolic pathway. The company is headquartered in Ponte Vedra, Florida, and its shares are listed on the NASDAQ.

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