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A Study to Evaluate Safety, Drug Levels and Effectiveness of CC-92480 (BMS-986348) in Combination With Other Treatments in Participants With Relapsed or Refractory Multiple Myeloma
NotableEnrollment target: 160 to 260Primary endpoints: 3 to 7 · Secondary endpoints: 9 to 12 · Site details revised at 3 of 17 sites · 1 morev17Show 4 more changesShow less
MinorEnrollment target: 220 to 160Eligibility criteria expanded, about 59 words · Site details revised at 4 of 17 sites · Study arms: 7 to 6v16Show 3 more changesShow less
MinorStudy sites: 10 to 11Start date changed from estimate of Oct 31, 2022 to Oct 18, 2022v6Show 1 more changeShow less
Start date changed from estimate of Oct 31, 2022 to Oct 18, 2022
MinorStudy sites: 9 to 10v5
NotableTrial status: Not Yet Recruiting to RecruitingPrimary and study completion dates: Apr 4, 2025 to Oct 12, 2026 · Start date: Aug 31, 2022 to Oct 31, 2022 · Study sites: 6 to 9v4Show 3 more changesShow less
Primary and study completion dates: Apr 4, 2025 to Oct 12, 2026
Start date: Aug 31, 2022 to Oct 31, 2022
Study sites: 6 to 9
MinorStudy sites: 5 to 6v3
NotableStart date: Jun 30, 2022 to Aug 31, 2022Study sites: 1 to 5v2Show 1 more changeShow less
Study sites: 1 to 5
MinorStudy First Submitted
Stopped: an ongoing trial was terminated, suspended or withdrawn.
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this study is to assess the safety, tolerability and preliminary effectiveness of CC-92480 (BMS-986348) in novel therapeutic combinations for the treatment of Relapsed or Refractory Multiple Myeloma (RRMM).