Approval Probability
TA Base Rate
Adjusted LOA
ML Risk
REC-7735 · 1 trial · 1 indication
| Arm | Type | Description |
|---|---|---|
| Phase 1A Dose Finding: REC-7735 | EXPERIMENTAL | Participants will receive REC-7735 twice daily (BID). |
| Phase 1B Dose Expansion/Optimization: REC-7735 | EXPERIMENTAL | Participants will receive REC-7735 BID. |
| Name | Type | Description |
|---|---|---|
| REC-7735 | DRUG | Oral |
Key Inclusion Criteria: * Participants have histologically-confirmed unresectable, locally advanced, or metastatic solid tumors which exhibit the PIK3CA H1047R mutation in tumor tissue and/or blood (circulating tumor deoxyribonucleic acid \[ctDNA\]). * For Phase 1A and planned monotherapy cohorts i...
| Company | Ticker | Trials | Lead Phase | Drugs |
|---|---|---|---|---|
| Merck & Co., Inc. | MRK | 2 | PHASE2 | Pembrolizumab, Gardasil 9 |
| Incyte Corporation | INCY | 1 | PHASE2 | Retifanlimab |
| Iovance Biotherapeutics Inc | IOVA | 2 | PHASE2 | Aldesleukin |
| Novartis AG Sponsored ADR | NVS | 1 | PHASE1 | KFA115 |
| AstraZeneca PLC | AZN | 1 | - | Trastuzumab deruxtecan |