Company guidance, FDA catalysts, dilution risk and cash runway, built from SEC, FDA and ClinicalTrials.gov filings and updated every day.
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| Drug | Indication | Most advanced trial | Status |
|---|---|---|---|
| Acellular Tissue Engineered Vessel | Vascular Injury | Phase 4 · NCT07762794 | Not yet recruiting |
| Human Acellular Vessel (HAV) | Renal Failure | Phase 3 · NCT02644941 | Completed |
| Hepatitis A Virus | Renal Failure | Phase 2 · NCT04135417 | Completed |
| Humacyte Coronary Tissue Engineered Vess | Coronary Artery Disease | Phase 2 · NCT07730528 | Not yet recruiting |
| HAVG | End-stage Renal Disease | Phase 1 · NCT01840956 | Completed |
| HAV implantation | Trauma | N/A · NCT05873959 | Completed |
Source: ClinicalTrials.gov trials sponsored by the company, one row per candidate at its most advanced registered trial. FDA approvals: Drugs@FDA. Wrong or missing drug? Report it
HUMA holds $79.9M in cash and short-term investments (as of Jun 30, 2026) and burns about $23.6M/quarter from operations, an estimated runway of 10.2 months at that rate (BioRadar estimate, not company guidance).
Source: SEC EDGAR (XBRL cash flow and financing filings). Dilution Watch: every company ranked → · Get an alert when HUMA files for a raise →
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