Cadrenal Therapeutics (CVKD) Registration filing summary
Event summary combining transcript, slides, and related documents.
Registration filing summary
21 Apr, 2026Company overview and business model
Late-stage biopharmaceutical company focused on therapies for immune and thrombotic conditions, with a primary focus on CAD-1005, a selective 12-LOX inhibitor for heparin-induced thrombocytopenia (HIT).
CAD-1005 has orphan drug and Fast Track designations from the FDA and orphan designation from the EMA.
Pipeline includes tecarfarin (oral VKA for patients with kidney dysfunction or LVADs) and frunexian (IV Factor XIa inhibitor for acute care settings).
Incorporated in Delaware in January 2022, with headquarters in Ponte Vedra, Florida.
Financial performance and metrics
Net tangible book value as of December 31, 2025: $2.7 million ($1.17 per share); pro forma net tangible book value: $6.3 million ($2.03 per share).
After offering and warrant exercises, as adjusted pro forma net tangible book value: $11.6 million ($2.73 per share).
Immediate dilution to new investors: $1.77 per share for Investor Warrant Shares, $2.895 for Placement Agent Warrant Shares.
Use of proceeds and capital allocation
No proceeds from resale of shares by selling stockholders; proceeds from 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.
Latest events from Cadrenal Therapeutics
- CAD-1005 offers a novel, upstream approach to HIT, aiming to improve outcomes and reduce costs.CVKD
Lytham Partners Spring 2026 Investor Conference28 May 2026 - First-in-class 12-LOX inhibitor CAD-1005 targets HIT, aiming for $1B+ market with Phase 3 in 2027.CVKD
Investor presentation7 May 2026 - Net loss narrowed and cash runway extended by $2.5M financing, enabling Phase 3 trial advancement.CVKD
Q1 20267 May 2026 - Phase 2 CAD-1005 data show >25% reduction in HIT thrombotic events; Phase 3 planning underway.CVKD
Q4 202531 Mar 2026 - CAD-1005 moves to phase III for HIT, aiming to address a critical unmet need with strong safety data.CVKD
Life Sciences Virtual Investor Forum12 Mar 2026 - Tecarfarin targets unmet anticoagulation needs in LVAD patients, with pivotal trials and partnerships ahead.CVKD
Sidoti Micro-Cap Virtual Conference2 Feb 2026 - Tecarfen aims to replace warfarin for high-risk heart patients, nearing FDA review with strong data.CVKD
Summer 2024 Investor Summit Virtual MicroCap Forum23 Jan 2026 - Tecarfarin aims to displace warfarin, with pivotal LVAD studies and strong regulatory momentum.CVKD
Lytham Partners Fall 2024 Investor Conference19 Jan 2026 - VLX-1005 and Tecarfarin lead a strategy to address unmet needs in rare anticoagulation markets.CVKD
2nd Annual Lytham Partners Healthcare Investor Summit15 Jan 2026