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NCT07105059PHASE1RECRUITING

A Study of Teclistamab and Mezigdomide in People With Multiple Myeloma

Teclistamab and Mezigdomide for Relapsed/Refractory Multiple Myeloma

Sponsor: Memorial Sloan Kettering Cancer Center + Bristol-Myers Squibb, Johnson & Johnson

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Key Facts

Study type
INTERVENTIONAL
Conditions
Multiple Myeloma
Interventions
Teclistamab, Mezigdomide
Enrollment
18 participants
Primary completion
Aug 2028
Study completion
Aug 2028
First posted
Aug 2025
Last updated
Feb 2026

Primary Endpoints (CT.gov)

Number of Participants With Dose Limiting Toxicity Assessed by CTCAE v5.0

Time frame: 1 year

Secondary Endpoints

Overall response rate

Eligibility Criteria

Inclusion Criteria: 1. Patients with relapsed or refractory multiple myeloma who have been treated with a proteasome inhibitor, an IMiD, and an anti-CD38 antibody. Patients who have been treated with at least 2 prior lines of therapy are eligible. Multiple myeloma is defined by the International Myeloma Working Group (IMWG) updated criteria. 2. Patients need to have measurable disease defined by one or more of the following: 1. Serum myeloma (M)-protein greater than or equal to 0.5 g/dL (5 g/L). 2. Urine M-protein greater or equal to 200 mg/24 h. 3. Involved light chain (either kappa or lambda) \>10 mg/dL with an abnormal kappa: lambda ratio 4. Plasmacytoma(s) that is new or definitely increased verified by imaging or biopsy. Increase is defined as a 50% and at least 1 cm increase as measured serially by the sum of the products of the cross-diameters of the measurable lesion. 5. A bone marrow biopsy demonstrating \>30% infiltration of clonal plasma cells. 3. Pat

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✦ Analyst Commentary

Expert commentary on why this trial matters and what to watch for.

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Source

Open on ClinicalTrials.gov