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Isatuximab With or Without Lenalidomide in Patients With High Risk Smoldering Multiple Myeloma (ISAMAR)

Smoldering Plasma Cell Myeloma Clinical Trial

Official title:
Phase II Trial of Isatuximab (SAR650984) With or Without Lenalidomide in Patients With High Risk Smoldering Multiple Myeloma (ISAMAR)

Clinical Trial Summary

This phase II trial studies how well isatuximab works in treating patients with high risk smoldering plasma cell myeloma. Immunotherapy with monoclonal antibodies, such as isatuximab, may induce changes in the body's immune system and may interfere with the ability of the tumor cells to grow and spread.

Clinical Trial Description

PRIMARY OBJECTIVE: - To determine the rate of response according to the International Myeloma Working Group Criteria. SECONDARY OBJECTIVES: - To determine progression free survival (PFS) at 2 years. - To determine overall survival (OS). - To determine duration of response (DOR). - To determine the clinical benefit rate (CBR). - To evaluate safety of single agent treatment in this population - To evaluate safety of single agent treatment in this population. - To evaluate the immunogenicity of isatuximab. OUTLINE: Patients receive isatuximab intravenously (IV) over 5 hours on day 1 of cycle 1, and over 3 hours thereafter on days 8, 15, and 22 of cycle 1, on days 1 and 15 of cycles 2-6, and on day 1 of subsequent cycles. Treatment repeats every 28 days for up to 30 cycles in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up every 6-12 months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02960555
Study type Interventional
Source M.D. Anderson Cancer Center
Contact
Status Active, not recruiting
Phase Phase 2
Start date February 8, 2017
Completion date June 30, 2025
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See also
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