
Sano Chemicals
OperatingSano Chemicals Inc
Retail & Consumer · Bryan, TX
Sano Chemicals is pioneering antifungal innovation with its flagship product, Occidiofungin - The Fungus Killer™. The first part of Phase 1 FDA human trials to treat recurrent vulvovaginal candidiasis (RVVC) has been successfully completed. Sano Chemicals is working to bring this innovative treatment to market, pending successful clinical trials and regulatory approval. RVVC is associated with chronic and recurrent yeast infections affecting up to 9 million women in the U.S. per year. FDA has granted Sano Chemicals qualified infectious disease product (QIDP) designation for its RVVC drug, which extends the expiration date on Occidiofungin patents for five years. Sano Chemicals believes it's poised to address a multi-billion U.S. market for treating recurrent and drug-resistant vaginal yeast infections.
Financials
FY2022–FY2025 · from SEC filings · hover any figure for its sourceFigures as reported by the issuer in the filing shown on hover. Each year’s pill shows the assurance level of its filed statements — audited, reviewed (CPA review, less than an audit), or unaudited, as the filing’s own report or certification states it. A dashed pill marked * is inferred instead: the SEC minimum for an offering that size, which the issuer may have exceeded. No pill means we couldn’t tell. Headcount is the filing’s point-in-time count, not a year-end average. Manually corrected figures are marked “Corrected”.
Valuation over rounds
Pre-money — the valuation set before each round’s money came inBlue bars are the pre-money valuation the company stated for a priced round.
Cap table
Share counts as of Apr 15, 2026| Class | Outstanding | Votes / share | Share of total | Last price |
|---|---|---|---|---|
| Series A Preferred Stockpreferred | 2,460,000 | 1 | 100.0% | — |
Sold to the crowd
- Reg CF · Jan 202536,793 shares at $5.43$199.8K· 74 investors
From the company's SEC filings: share counts per class, each class's voting and conversion terms, and the holders of 20% or more that Form C requires (officers and 10%+ holders on Form 1-A). Filings name only large holders, so most owners — including crowd investors — are not listed, and a holder's percentage may be of its own class rather than of the whole company. Prices and crowd share counts are in today's share terms — adjusted for splits and conversions since they were sold. Hover a figure for its filing.
Fundraising history
Team
17 people
Dr. Miles leads women’s health initiatives at Sano Chemicals Inc, where she leads business development efforts on female health products. Dr. Miles is an entrepreneur with over 30 years of clinical experience. She has a deep understanding of medical disorders and the need for new pharmacologic therapies to treat infectious diseases. She served on the Board of the Mississippi Gulf Coast Women’s Medical Association. She has a deep understanding of the clinical impact of antibiotic resistance, and particularly its impact on women’s health. She was the first woman Chief Fellow in her Pulmonary Disease Fellowship. Dr Miles has published research on clinical infectious diseases. Dr. Miles managed the manufacturing operations of Miles Osborn Inc. for over a decade. Dr. Miles received her Doctor of Osteopathy from Ohio University / College of Osteopathic Medicine. In addition to working approximately 15 hours a week for Sano Chemicals, Dr. Miles also works 30-50 hours per week as Owner, Physician, Sleep Center Director for Pulmonary and Sleep Medicine Sleep Lab.

Dr. Smith has over 20 years of scientific, operational, strategic and management experience in the biotech industry. He is a Full Professor in Biology and has been involved in the formation, product development, and leadership of several biotechnology companies over the last two decades. Dr. Smith holds more than 25 patents associated with antimicrobial and cancer therapeutics. He has authored over 50 peer-reviewed publications covering topics on drug discovery and antibiotic development. He previously held leadership roles as Product Leader for Oragenics Inc., contributing to the development of its antimicrobial product line. These product lines were used to leverage investments from government, private, and public sectors. In the early 2000s, he was Vice President of Ivigene Inc., which used a proprietary drug discovery platform for the identification of novel protein targets for vaccines and diagnostics products. Dr. Smith was the founder of Biotech Analyst Group, which provided an in-depth analysis of technologies and their related patents. He served as an Executive Director of the Able Trust Foundation in Tallahassee, FL for five years through a gubernatorial appointment. Dr. Smith has a Doctorate degree in Biochemistry from the College of Medicine at the University of Florida and an M.B.A. degree in Finance and Competitive Strategy from Warrington College of Business. Dr. Smith leads the overall strategy for Sano as well as runs the research and development team at the Sano Chemicals research facilities in Bryan, TX. In addition to working approximately 20 hours a week for Sano Chemicals, Dr. Smith also works 30-40 hours per week as a Professor for Texas A&M University.

Mr. Goodstein graduated with a BA in Accounting from the University of Washington in 1983. He has worked in public accounting and internal auditing, in the University of Copenhagen, Denmark International Program, and as a CPA in Anchorage Alaska. He is a QuickBooks Certified ProAdvisor, member of the CFO Leadership Council, and a Mass Challenge Austin Mentor.

Dr. Austin is a long-standing researcher in rare infections. Dr. Austin has over thirty years of mycology experience. He was the director of the Microbiological Diagnostic Laboratory at the College of Veterinary Medicine at Mississippi State University. He is a founding member of Sano Chemicals and supports drug development and fund-raising efforts.

Dr. Atiee received his medical degree from UTHSC San Antonio and has been involved in clinical pharmacology research for 23 years. He was Medical Director and Principal Investigator of Worldwide Clinical Trials’ 300 bed facility in San Antonio, Texas. He has worked as an Associate Medical Director for the clinical trial CRO Icon Development Solutions. He has performed and prepared IND applications for over 300 Phase 1 and 2 trials in multiple therapeutic areas. Dr. Atiee is instrumental to Sano where he leads the design and strategy of clinical protocols for our clinical trials.

Dr. Orugunty has two doctorate degrees from University of Florida in Medicinal Chemistry and Organic Chemistry. He is experienced with bioanalytical and analytical chemistry. He has extensive product development experience with his tenure at Cerilliant (EMD MilliporeSigma). Further, Ravi has extensive experience in bioanalytical method development and validation gained from his tenure with Worldwide Clinical Trials Inc. Dr. Orugunty's efforts will facilitate the development of novel therapeutic products in Sano's pipeline.

Mr. Tenorio graduated with a B.S. degree in the Department of Biology at Texas A&M University in 2018. He has experience working with large bioreactors. He brings GMP manufacturing practices and experience in upstream and downstream manufacturing processes. Has extensive experience in establishing and monitoring standard operating procedures and batch production records.

Mrs. Nair is responsible for safeguarding that products meet established quality standards. She identifies any potential issues in documentation or practices within the manufacturing processes. She monitors and maintains quality throughout the production cycle ensuring compliance with industry regulations.
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Mr. Cao graduated with a B.S. degree in the Department of Biology at Texas A&M University in 2017. He has analytical chemistry and drug product formulation experience. He has bioanalytical method development experience used in validating processes in downstream manufacturing of drug products.

As a Principal Investigator, Shien Lu has been working on bacterial genetics of biosynthesis of antimicrobial compounds at Mississippi State University since 2004. Prior to joining the faculty of Mississippi State, he was involved in genetic analysis of antimicrobial biosynthesis of Pseudomonas as a primary investigator at Washington State University and Texas A&M University since 1998. Dr. Lu brings extensive experience in research and development of antimicrobial products produced by bacteria.

Dr. Pruett has over thirty-five years of experience with rodent models of infectious diseases and cancer with emphasis on the immune system and toxicology. He brings extensive experience in toxicological and efficacy studies for the development of new therapeutics. He is a founding member of Sano Chemicals and is a former Vice Dean of the College of Veterinary Sciences. Prior to this, he was the Department Chair for the Department of Basic Sciences at the College of Veterinary Medicine at Mississippi State University.

Dr. Hiebert has over 30 years of clinical experience with a deep understanding of infectious diseases. He received his MD from Texas Tech University and his B.S. in geography. He is a specialist in pulmonary, critical care, and sleep medicine. He has a DVM from the College of Veterinary Medicine at Mississippi State University.
Names and titles as disclosed on StartEngine, SEC Form C. Bios and photos come from the platform campaign page and may be out of date.
Reg CF annual-report compliance
Filed 2 of 2 annual reports (FY2024–FY2025)
Reg CF issuers must file a Form C-AR each year until a Rule 202(b) termination trigger is met.
SEC filings
- Form C-ARApr 15, 20260002007816-26-000005EDGAR
- Form C-UMay 8, 20250001665160-25-001033EDGAR
- Form C/AApr 10, 20250001665160-25-000609EDGAR
- Form C-ARApr 10, 20250001665160-25-000611EDGAR
- Form C-UJan 24, 20250001665160-25-000137EDGAR
- Form CJan 10, 20250001665160-25-000042EDGAR
- Form DMay 16, 20240002007816-24-000002EDGAR
- Form DJan 17, 20240002007816-24-000001EDGAR
About this data. Figures are compiled from public sources — SEC EDGAR filings (Form C, C-AR, 1-A, 1-K) and funding-platform pages — and may be delayed, incomplete, or restated by the issuer. Financial statements are as reported by the issuer; each year is labeled with its assurance level (audited / reviewed / unaudited). A valuation cap is the conversion ceiling of a SAFE or convertible note, not an agreed company valuation; post-money figures are computed as pre-money plus amount raised and are not a traded price. Crowdonomics is not a broker-dealer, funding portal, or investment adviser; nothing here is investment advice or an offer to sell securities. Verify all figures against the linked EDGAR filings.