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 |
|---|---|---|---|
| Fc-Gamma Receptor III | High-risk Myelodysplastic Syndromes | Phase 1/2 · NCT03214666 | Terminated |
| Anti-B7-H3/IL-15/Anti-CD16 Trispecific N | Tri-specific Killer Engager | Phase 1 · NCT07541573 | 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
GTBP holds $5M in cash and short-term investments (as of Jun 30, 2026) and burns about $3.4M/quarter from operations, an estimated runway of 4.4 months at that rate (BioRadar estimate, not company guidance).
Dilution pressure: 45 · Elevated
These factors raise substantial doubt about the Company’s ability to continue as a going concern within one year of the date that the financial statements are issued.10-Q, Aug 2026
Recent financing filings on SEC EDGAR:
Source: SEC EDGAR (XBRL cash flow and financing filings). Dilution Watch: every company ranked → · Get an alert when GTBP files for a raise →
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