A Randomized, Double-blind, Parallel-group Study to Compare Pharmacokinetics of GME751 (Proposed Pembrolizumab Biosimilar) and US-licensed and EU Authorized Keytruda® in Participants With Stage II and III Melanoma Requiring Adjuvant Treatment With Pembrolizumab
Latest Information Update: 09 May 2025
At a glance
- Drugs GME 751 (Primary) ; Pembrolizumab
- Indications Malignant melanoma
- Focus Pharmacokinetics
- Sponsors Sandoz
Most Recent Events
- 01 May 2025 Planned End Date changed from 20 Jun 2025 to 1 Jul 2026.
- 01 May 2025 Planned primary completion date changed from 20 Jun 2025 to 1 Jul 2026.
- 29 May 2024 Status changed from not yet recruiting to recruiting.