CytoDyn Inc. (CYDY)
Pharmaceutical Preparations · market cap $290M · as of 2026-07-09
Research and calibrated estimates, not financial advice — verify before acting.
No upcoming catalysts in our calendar.
| Asset | Phase | Indication |
|---|---|---|
| leronlimab 700 mg | Phase 2 | Nonalcoholic Steatohepatitis (NASH) |
| PRO 140 (350 mg) | Phase 3 | HIV |
| Leronlimab (700mg) | Phase 2 | Coronavirus Disease 2019 |
| PRO 140 (humanized monoclonal antibody to CCR5) | Phase 2 | HIV -1 Infection |
| Optimized Background Regimen | Phase 3 | HIV |
| PRO 140 | Phase 3 | HIV-1-infection |
| Leronlimab | Phase 2 | Solid Tumor, Adult |
| 350 mg leronlimab | Phase 2 | Metastatic Colorectal Cancer (mCRC) |
Daily closes through 2026-09-30. Realized vol annualized; max drawdown over ~2 years.
The full dossier is a Pro feature
Thesis, bull & bear, the if-approved scenario, financials, smart-money signals and risks — compiled by CeliA. The catalyst path & pipeline above are free.
- SEC filings — EDGAR filings for CYDY (10-K, 10-Q, S-3, 13D/G, Form 4)
- Clinical trials — 8 registered trials on ClinicalTrials.gov (per-trial NCT links in the pipeline)
- Market & financial data — SEC EDGAR (XBRL filings, Form 4), Yahoo Finance, Nasdaq — prices, statements, key metrics, insider & institutional filings.
- Regulatory — openFDA, FDA advisory & PDUFA calendars.
Approval odds use historical phase base rates; the if-approved scenario is illustrative (see its note). Figures trace to the sources above — verify before acting.
Data from CatalystAlert (ClinicalTrials.gov, SEC EDGAR, openFDA, market-data providers). Compiled by CeliA. Not financial advice.
