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 |
|---|---|---|---|
| WVE-210201 | Duchenne Muscular Dystrophy | Phase 2/3 · NCT03907072 | Terminated |
| SAD: 30mg WVE-003 | Huntington Disease | Phase 1/2 · NCT05032196 | Completed |
| WVE-004 | ALS | Phase 1/2 · NCT04931862 | Terminated |
| WVE-006 | Alpha-1 Antitrypsin Deficiency | Phase 1/2 · NCT06405633 | Active not recruiting |
| WVE-007 | Overweight and Obesity | Phase 1/2 · NCT06842186 | Recruiting |
| WVE-120101 | Huntington's Disease | Phase 1/2 · NCT03225833 | Terminated |
| WVE-120102 | Huntington's Disease | Phase 1/2 · NCT03225846 | Terminated |
| WVE-N531 | Duchenne Muscular Dystrophy | Phase 1/2 · NCT04906460 | Recruiting |
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
WVE holds $490.6M in cash and short-term investments (as of Jun 30, 2026) and burns about $56.6M/quarter from operations, an estimated runway of 26 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 WVE files for a raise →
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