drugset / Trial / NCT02812706

Isatuximab Single Agent Study in Japanese Relapsed AND Refractory Multiple Myeloma Patients

NCT02812706

Phase 1/2 Completed 36 enrolled Sanofi
Non-randomizedSequentialOpen-labelTreatment

Summary

Primary Objectives: * Phase I: To evaluate safety and tolerability of isatuximab in Japanese participants with relapsed and refractory multiple myeloma. * Phase II: To evaluate efficacy of isatuximab at recommended dose and to further evaluate the overall response rate (ORR) of isatuximab in Japanese participants with relapsed and refractory multiple myeloma. Secondary Objectives: * To evaluate the safety including immunogenicity of isatuximab. The severity, frequency and incidence of all adverse events were assessed. * To evaluate the pharmacokinetic (PK) profile of isatuximab in the proposed dosing schedule. * To assess the efficacy using International Myeloma Working Group (IMWG) uniform response criteria. * To assess the relationship between Baseline cluster of differentiation 38 (CD38) receptor density on multiple myeloma cells and efficacy.

Timeline

Start
2016-09-05
Primary completion
2018-07-31
Completion
2022-09-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Isatuximab Monoclonal antibody 10 mg/kg Intravenous
Subject Isatuximab Monoclonal antibody 20 mg/kg Intravenous

Indications