drugset / Trial / NCT03913923
Study of Efficacy and Safety of BCD-217 (Anti-CTLA-4 and Anti-PD-1) Followed By BCD-100 (Anti-PD-1) Versus BCD-100 Monotherapy as First-Line Treatment in Patients With Unresectable or Metastatic Melanoma
RandomizedParallel-groupDouble-blindTreatment
Summary
This is a multicenter randomized double-blind placebo-controlled phase II clinical trial. The purpose of this trial is to evaluate efficacy and safety of therapy consisting of BCD-217 (fixed dose combination of anti-CTLA-4 and anti-PD-1 monoclonal antibodies) and sequential BCD-100 (anti-PD-1 monoclonal antibody) versus BCD-100 monotherapy as first-line treatment in patients with treatment-naïve unresectable or metastatic melanoma.
Timeline
- Start
- 2019-07-01
- Primary completion
- 2023-07
- Completion
- 2023-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | BCD-100 | Monoclonal antibody | 1 mg/kg | Intravenous |
| Subject | BCD-217 | Monoclonal antibody | 1 mg/kg | Intravenous |
| Subject | BCD-217 | Monoclonal antibody | 3 unknown | Intravenous |