Approval Probability 71%
TA Base Rate26%
Adjusted LOA41%
ML RiskLOW_RISK
| NCT ID | Title | Phase | Status | Enrollment | Velocity | Design | Start | Completion | Last Updated | Sites | Countries |
|---|---|---|---|---|---|---|---|---|---|---|---|
| NCT06781983 | Safety and Tolerability of IPH4502 in Patients With Advanced Solid Tumors | PHASE1 | RECRUITING | 145 | — | — | Jan 24, 2025 | Apr 1, 2029 | Jan 7, 2026 | 7 | United States, France |
To evaluate the incidence of AEs, SAEs, TEAEs, and DLTs.
| Arm | Type | Description |
|---|---|---|
| IPH4502 Monotherapy | EXPERIMENTAL | - |
| Name | Type | Description |
|---|---|---|
| IPH4502 | DRUG | Part 1 (dose escalation) and Part 2 (dose optimization) |
Main Inclusion Criteria: * Histologically confirmed, unresectable, locally advanced or metastatic solid tumors that are known to express Nectin-4 * Prior systemic treatment for locally advanced or metastatic disease, yet no therapy with demonstrated clinical benefit for the tumor type is available....
| Company | Ticker | Trials | Lead Phase | Drugs |
|---|---|---|---|---|
| Merck & Co., Inc. | MRK | 2 | PHASE2 | pembrolizumab, V503, GARDASIL |
| Incyte Corporation | INCY | 1 | PHASE2 | Chemotherapy, Retifanlimab |
| Novartis AG Sponsored ADR | NVS | 1 | PHASE1 | KFA115, pembrolizumab |
| Iovance Biotherapeutics Inc | IOVA | 2 | PHASE2 | E7 TCR-T cells, Aldesleukin |
| AstraZeneca PLC | AZN | 1 | — | Trastuzumab deruxtecan |