Approval Probability
TA Base Rate
Adjusted LOA
ML Risk
Ivonescimab combined with Cadonilimab · 1 trial · 1 indication
ORR per RECIST v1.1 by investigator
Adverse events (AEs) as characterized by type, incidence, severity, seriousness, and relationship to study treatment
| Arm | Type | Description |
|---|---|---|
| Ivo 1 + Cado | EXPERIMENTAL | Ivonescimab (dose level 1) + Cadonilimab |
| Ivo 2 + Cado | EXPERIMENTAL | Ivonescimab (dose level 2) + Cadonilimab |
| Ivo + Ipi | EXPERIMENTAL | Ivonescimab + Ipilimumab |
| Ivo | EXPERIMENTAL | Ivonescimab |
| Nivo + Ipi | ACTIVE_COMPARATOR | Nivolumab + Ipilimumab |
| Name | Type | Description |
|---|---|---|
| Ivonescimab (dose level 1) combined with Cadonilimab | DRUG | Subjects will receive Ivonescimab (dose level 1) combined with Cadonilimab via intravenous infusion (IV) up to 2 years. |
| Ivonescimab (dose level 2) combined with Cadonilimab | DRUG | Ivonescimab (dose level 2) combined with Cadonilimab via intravenous infusion (IV) up to 2 years. |
| Ivonescimab combined with Ipilimumab | DRUG | Ivonescimab combined with Ipilimumab via intravenous infusion (IV) up to 4 cycles. Afterward, Ivonescimab for maintenance treatment up to 2 years total. |
| Ivonescimab | DRUG | Ivonescimab monotherapy via intravenous infusion (IV) up to 2 years. |
| Nivolumab combined with Ipilimumab | DRUG | Nivolumab combined with Ipilimumab via intravenous infusion (IV) up to 4 cycles. Afterward, Nivolumab will be used for maintenance treatment up to 2 years total. |
Inclusion Criteria: 1. Able to understand and voluntarily sign a written informed consent form, which must be signed prior to the performance of the designated study procedures required by the study. 2. Age ≥ 18 years both male and female. 3. Karnofsky Performance Status Score (KPS) ≥ 70%. 4. Expec...