| Metric | Period | Current guidance |
|---|---|---|
| Cash runway | As of September 30, 2025 | $16.9M in cash and $11.1M working capital following the September public offering; company continued to require additional capital |
| elraglusib mPDAC program (Actuate-1801) | Ongoing | Continued follow-up on the Phase 2 first-line mPDAC study that met its primary overall-survival endpoint |
| Metric | YoY | Note |
|---|---|---|
| Research & development expense | $2.2M (vs $3.8M) | Lower clinical spend after completion of Phase 2 mPDAC enrollment. |
| General & administrative expense | $3.3M (vs $1.6M) | Higher public-company and personnel costs. |
| Net loss | $5.4M (vs $6.0M) | Lower R&D partly offset by higher G&A. |
| Diluted net loss per share | $(0.25) | Loss per share on 21.4M weighted-average shares outstanding. |
| Cash & cash equivalents | $16.9M | Boosted by ~$15.6M net proceeds from the September 2025 public offering. |
| Topic | Previous mention | Current period | Trend |
|---|---|---|---|
| Balance sheet | $6.5M cash; working-capital deficit | $16.9M cash; $11.1M working capital after September offering | Up |
| mPDAC program | Positive Phase 2 topline | Continued advancement in first-line mPDAC | Steady |
| Going concern | Runway into October 2025 | Doubt persists; accumulated deficit $150.1M | Steady |