Advanced Renal Cell Cancer Combination ImmunoThErapy Clinical Trial
Summary
This study is a randomized, open label, multicenter Phase II trial to evaluate the efficacy and safety of botensilimab (a novel Fc enhanced Tree depleting anti-CTLA4) and balstilimab (a novel anti-PD1) relative to ipilimumab and nivolumab in treatment naïve patients with metastatic ccRCC. The study will plan to enroll 120 eligible patients randomized in a 2:1 fashion to Arm A and Arm B. Patients in all IMDC Risk Groups are included. This study utilizes a Simon's two stage design which is described in the protocol. Patients randomized to Arm A will receive botensilimab in combination with balstilimab. Patients randomized to Arm B will receive ipilimumab in combination with nivolumab. Study treatment on both arms will continue until toxicity, disease progression or a maximum of 96 total weeks (12 weeks induction, 84 weeks maintenance).
Timeline
- Start
- 2023-09-25
- Primary completion
- 2026-11-10
- Completion
- 2027-11-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Balstilimab | Monoclonal antibody | 450 mg | Intravenous |
| Subject | Botensilimab | Monoclonal antibody | 75 mg | Intravenous |
| Comparator | Ipilimumab | Monoclonal antibody | 1 mg/kg | Intravenous |
| Comparator | Nivolumab | Monoclonal antibody | 480 mg | Intravenous |