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  • NCT03486067

Active, Not Recruiting

Study of CC-93269, a BCMA x CD3 T Cell Engaging Antibody, in Participants With Relapsed and Refractory Multiple Myeloma - CC-93269-MM-001

Updated: 17 February, 2025   |   ClinicalTrials.gov

Celgene Corporation, a wholly owned subsidiary of Bristol-Myers Squibb Company

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CONSIDERING THIS TRIAL?
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Use the Study Participant's Guide to navigate the process of participating in a clinical trial. Understand key factors to consider before deciding and get questions to ask your healthcare team.
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Trial Details

  • Phase 1

    Phase

  • Gender(s)

  • 18+

    Age Range

  • Active, Not Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Experimental: Administration of CC-93269
Drug: CC-93269

Key Eligibility Criteria

Inclusion Criteria: - History of multiple myeloma with relapsed and refractory disease - Eastern Cooperative Oncology Group Performance Status of 0 or 1 - Must have measurable disease as determined by the central laboratory Exclusion Criteria: - Symptomatic central nervous system involvement of multiple myeloma - Prior autologous stem cell transplant ≤ 3 months prior - Prior allogeneic stem cell transplant with either standard or reduced intensity conditioning ≤ 12 months prior - History of concurrent second cancers requiring active, ongoing systemic treatment Other protocol-defined inclusion/exclusion criteria apply

If you want to report a side effect, you can report directly to the Danish Medicines Agency via the website www.meldenbivirkning.dk
We recommend that you also contact BMS to report side effects.
Side effects and other reportable events are defined here
Report side effects or product quality complaints: Medical Information

466-DK-2200001