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Active, Not Recruiting

A Study of CC-99712, a BCMA Antibody-Drug Conjugate, in Participants With Relapsed and Refractory Multiple Myeloma - CC-99712-MM-001

Updated: 29 January, 2024   |   ClinicalTrials.gov

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

Print Friendly Summary

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.

Trial Details

  • Phase 1

    Phase

  • Gender(s)

  • 18+

    Age Range

  • Active, Not Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Experimental: Arm 1 (CC-99712 monotherapy)
Drug: CC-99712
Experimental: Arm 2 (CC-99712 and BMS-986405 combination)
Drug: CC-99712, BMS-986405

Key Eligibility Criteria

Participants must satisfy the following criteria to be enrolled in the study: Inclusion - Participant is ≥ 18 years of age at the time of signing the ICF. - Participant has a history of multiple myeloma (MM) with relapsed and/or refractory disease - Participant must have measurable disease. - Participant has an Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 or 1. Exclusion Criteria - Participant has symptomatic central nervous system involvement of MM. - Participant had a prior autologous stem cell transplant ≤ 3 months prior to starting CC-99712. - Participant had a prior allogeneic stem cell transplant with either standard or reduced intensity conditioning ≤ 6 months prior to starting CC-99712 or is on systemic immunosuppression for graft-versus host disease. - Subject is a pregnant or lactating female. - Subject has known human immunodeficiency virus (HIV) infection. - Subject has active hepatitis B or C (HBV/HCV) infection. Other protocol-defined inclusion/exclusion criteria apply

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Have questions? Live support is available 24/7 - Call 833-673-6134 Or Email Us

Have questions? Live support is available 24/7 -
Call 833-673-6134 Or Email Us