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Sub-study of Belantamab Mafodotin (GSK2857916) in Combination With Nirogacestat in Participants With RRMM
The primary purpose is to determine the safety and tolerability of belantamab mafodotin in combination with nirogacestat and to establish the recommended Phase 2 dose for combination treatment to explore in the cohort expansion (CE) phase in participants with RRMM. This study is a sub study of the Master protocol (NCT04126200).
Details
| Lead sponsor | GlaxoSmithKline |
|---|---|
| Phase | PHASE1, PHASE2 |
| Status | ACTIVE_NOT_RECRUITING |
| Enrolment | 106 |
| Start date | Mon Jun 08 2020 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Thu Mar 11 2027 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Multiple Myeloma
Interventions
- Belantamab mafodotin
- Nirogacestat
Countries
France, Netherlands, Russia, Greece, Sweden, Germany, Poland, Norway, South Korea, Canada, Australia, United States, Spain