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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| NCT05297903 | XmAb20717 in Advanced Biliary Tract Cancers | PHASE2 | ACTIVE NOT_RECRUITING | 27 | — | — | Apr 11, 2022 | Dec 2, 2026 | Sep 15, 2025 | 1 | United States |
Proportion of participants with the best response being complete response (CR) or partial response (PR)
| Arm | Type | Description |
|---|---|---|
| XmAb20717 | EXPERIMENTAL | Study participants will receive the recommended phase II dose (10mg/kg) of XmAb20717 by intravenous infusion on days 1 and 15 of a 28-day cycle for up to 2 years. |
| Name | Type | Description |
|---|---|---|
| XmAb20717 | DRUG | 10mg/kg IV |
Inclusion Criteria: 1. Provision of signed and dated informed consent form 2. Stated willingness to comply with all study procedures and availability for the duration of the study 3. Male or female, aged \> 18 years of age 4. Patient must have advanced biliary tract cancers (BTC) including intrahep...