| Metric | Period | Current guidance |
|---|---|---|
| Cash runway | As of September 30, 2025 | $134.4M in cash, equivalents and marketable securities; funds operations into Q2 2027 |
| ACR-368 registrational-intent / confirmatory trial design | H2 2025 | Update expected in the second half of 2025 |
| ACR-2316 Phase 1 initial data | H2 2025 | Initial clinical data expected in the second half of 2025 |
| Metric | YoY | Note |
|---|---|---|
| Research & development expense | $13.6M (vs $18.9M) | Fewer scheduled and incurred milestones and prioritization of endometrial cancer in the ACR-368 trial. |
| General & administrative expense | $6.0M (vs $6.3M) | Materially consistent year over year. |
| Net loss | $18.2M (vs $22.4M) | Lower R&D spend; loss from operations of $19.7M partly offset by $1.5M interest income. |
| Cash, equivalents & marketable securities | $134.4M | As of September 30, 2025; funds operations into Q2 2027. |
| Diluted net loss per share | $(0.47) | On 38.6M weighted-average shares outstanding. |
| Topic | Previous mention | Current period | Trend |
|---|---|---|---|
| ACR-368 in endometrial cancer | Arm 3 initiated | Arm 3 (ULDG, biopsy-independent) actively enrolling and dosing | Up |
| ACR-2316 Phase 1 | Confirmed PR in endometrial cancer | Tumor shrinkage and confirmed PR across several solid tumor types; preparing initial data disclosure | Up |
| Cash runway | $147.6M into Q2 2027 | $134.4M into Q2 2027 | Steady |