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Sub-study of Belantamab Mafodotin (GSK2857916) in Combination With Nirogacestat in Participants With RRMM

NCT07084896 PHASE1, PHASE2 ACTIVE_NOT_RECRUITING

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 sponsorGlaxoSmithKline
PhasePHASE1, PHASE2
StatusACTIVE_NOT_RECRUITING
Enrolment106
Start dateMon Jun 08 2020 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionThu Mar 11 2027 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

France, Netherlands, Russia, Greece, Sweden, Germany, Poland, Norway, South Korea, Canada, Australia, United States, Spain