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 |
|---|---|---|---|
| 514G3 (10 mg/kg) plus standard IV antibi | Staphylococcus Aureus Bacteremia | Phase 1/2 · NCT02357966 | Completed |
| 514G3 (40 mg/kg) plus standard IV antibi | Staphylococcus Aureus Bacteremia | Phase 1/2 · NCT02357966 | Completed |
| Natrunix | Rheumatoid Arthritis | Phase 2 · NCT05363891 | Completed |
| Phase I: XB2001 1000 mg | Pancreatic Cancer | Phase 1/2 · NCT04825288 | Completed |
| Phase II: XB2001 1000 mg | Pancreatic Cancer | Phase 1/2 · NCT04825288 | Completed |
| Vilamakitug | Axial Spondyloarthritis | Phase 2 · NCT06526377 | Not yet recruiting |
| Hutrukin | Pharmacokinetics | Phase 1 · NCT05098080 | Completed |
Also used in these trials (approved or third-party drugs, not XBIT's own candidates): Methotrexate.
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
XBIT holds $109.5M in cash and short-term investments (as of Jun 30, 2026) and burns about $6.7M/quarter from operations, an estimated runway of 48.7 months at that rate (BioRadar estimate, not company guidance).
Dilution pressure: 0 · Low
Recent financing filings on SEC EDGAR:
Source: SEC EDGAR (XBRL cash flow and financing filings). Dilution Watch: every company ranked → · Get an alert when XBIT files for a raise →
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