Investor Relations - Arianova Bio

Investment Opportunity

A Proven Treatment.
A Clear Pathway.

Arianova Bio is seeking strategic investment to complete the FDA validation pathway for a herbal wound care ointment with a documented track record of success in Iran. We are not starting from scratch — we are bringing a proven solution to the world's largest healthcare market.

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The Market Opportunity

Chronic wound care is a massive, underserved market with growing demand for effective, natural alternatives.

$20B+
U.S. Wound Care Market

Projected to exceed $20 billion by 2027, driven by diabetes and aging population

8.2M
Chronic Wound Patients

Americans suffering from chronic wounds, diabetic foot ulcers, and severe burns annually

1–3 wks
Proven Healing Time

Documented healing outcomes in Iranian patients using our herbal ointment formulation

Milestones & Roadmap

We have already achieved critical early milestones. Your investment accelerates the path to FDA approval.

Proven clinical use in IranAchieved

Hundreds of patients treated for chronic wounds, diabetic foot ulcers, and burns with 1–3 week healing times.

$10K USTAAR Grant awardedAchieved

University of Miami Venture Catalyst funding secured, validating our commercial potential.

CIC St. Louis partnershipAchieved

Research partnership established at a world-class innovation center for in vitro validation.

In vitro testing underwayAchieved

Wound scratch assay, cell viability, proliferation, cytotoxicity, antimicrobial, and anti-inflammatory studies in progress.

Complete FDA validation package

Full in vitro data package required for FDA pre-submission meeting and IND application.

FDA pre-submission meeting

Formal engagement with FDA to align on approval pathway and clinical trial requirements.

Phase I/II clinical trials

U.S.-based clinical trials to confirm safety and efficacy for FDA approval.

FDA approval & U.S. market launch

Bring a proven, natural wound care solution to the multi-billion dollar U.S. wound care market.

Use of Funds

We are seeking $500,000 in seed funding to complete the FDA validation pathway and prepare for clinical trials.

40%In Vitro Testing Completion

Finalize all 6 validation assays at CIC St. Louis

25%FDA Regulatory Affairs

Pre-submission meetings, IND application preparation

20%Clinical Trial Preparation

Protocol design, site selection, IRB approval

15%Operations & IP Protection

Patent filings, team expansion, overhead

Ready to Invest in the Future of Wound Care?

We welcome conversations with angel investors, family offices, biotech VCs, and strategic partners who share our vision of bringing proven, natural therapeutics to the U.S. market.