Skip to main content

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

Recruiting · Phase 1, Phase 2 · NCT05372354

Conditions: Multiple Myeloma

At a glance

Research payments reported, 2025
$402,716
U.S. investigators named
4
Sites paid
4
Planned or actual enrollment
260

About the trial

Sponsor
Bristol-Myers Squibb
Tested
CC-92480 (drug), Tazemetostat (drug), BMS-986158 (drug), Trametinib (drug), Dexamethasone (drug)
Dates
Started 2022-10-18; completion 2026-10-12
Results posted
Not yet

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).

From ClinicalTrials.gov, last updated 2025-09-05. Full record, eligibility and contacts (opens in a new tab)

Industry funding

E.r. Squibb & Sons, L.l.c. reported $402,716 in research payments for this study in 2025 (4 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

  • Uab Comprehensive Cancer Center $277,548
  • John Theurer Cancer Center $48,979
  • Dana-Farber Cancer Institute $43,537
  • Johns Hopkins Medicine - the Sidney Kimmel Comprehensive Cancer Center $32,653

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.