Cadrenal Therapeutics (Nasdaq: CVKD) Announces Closing of Initial Public Offering
Cadrenal Therapeutics (Nasdaq: CVKD) announced the closing of its initial public offering, successfully selling 1,400,000 shares at $5.00 each, raising $7 million before expenses. The offering commenced trading on the Nasdaq Capital Market on January 20, 2023. The firm has granted underwriters a 45-day option to purchase an additional 210,000 shares. Cadrenal is focused on developing tecarfarin, a novel therapy for preventing blood clots in patients with end-stage renal disease and atrial fibrillation, holding orphan drug and Fast Track designations. The press release also contains forward-looking statements regarding future expectations.
- Raised $7 million from the IPO, which could support further development of tecarfarin.
- Tecarfarin has orphan drug and Fast Track designations, indicating its potential value in treating niche markets.
- Potential dilution of shares if underwriters exercise their option for additional shares.
The Company's common stock began trading on the Nasdaq Capital Market on
A registration statement on Form S-1 (File No. 333-267562) relating to these shares was filed with the
This press release does not constitute an offer to sell or the solicitation of an offer to buy these securities, nor will there be any sale of these securities in any state or jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction.
ABOUT CADRENAL THERAPEUTICS, INC.
Cadrenal Therapeutics is focused on developing tecarfarin, a novel cardiorenal therapy with orphan drug and Fast Track designations for the prevention of systemic thromboembolism (blood clots) of cardiac origin in patients with end-stage renal disease, or ESRD, and atrial fibrillation (irregular heartbeat), or AFib. Tecarfarin is a Vitamin K antagonist oral anticoagulant designed to target a different pathway than the most commonly prescribed drugs used in the treatment of thrombosis and AFib. Tecarfarin has been evaluated in eleven 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, please visit: www.cadrenal.com.
Safe Harbor Statement
Any statements contained in this press release about future expectations, plans and prospects, as well as any other statements regarding matters that are not historical facts, may constitute "forward-looking statements." The words "anticipate," "believe," "continue," "could," "estimate," "expect," "intend," "may," "plan," "potential," "predict," "project," "should," "target," "will," "would" and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Actual results may differ materially from those indicated by such forward-looking statements as a result of various important factors, including factors discussed in the "Risk Factors" section of the initial public offering prospectus filed with the
For more information, please contact:
For Underwriter Inquiries:
949-502-4408
keith@boustead1828.com
Cadrenal Therapeutics:
858-337-0766
press@cadrenal.com
Investors:
602-889-9700,
CVKD@lythampartners.com
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