drugset / Trial / NCT04855136

Safety and Efficacy of bb2121 (Ide-cel) Combinations in Multiple Myeloma

NCT04855136

Phase 1 Terminated 21 enrolled Celgene Corporation
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a global, open-label, multi-arm, multi-cohort, multi-center, phase 1/2 study to determine the safety, tolerability, efficacy, PK of bb2121 in combination with other therapies in adult subjects with R/RMM. The following combinations will be * Arm A will test bb2121 in combination with CC-220 (± low-dose dexamethasone) * Arm B will test bb2121 in combination with BMS-986405 (JSMD194) Combination agents being tested may be administered before, concurrently with and/or following (ie, maintenance) bb2121 infusion. The study will consist of 2 parts: dose finding (Phase 1) and dose expansion (Phase 2). Dose expansion may occur in one or more arms.

Timeline

Start
2021-06-01
Primary completion
2025-04-25
Completion
2025-04-25

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-986405 Unknown
Subject Iberdomide Small molecule
Subject idecabtagene vicleucel Cell therapy 4.5e+08 cells

Indications