drugset / Trial / NCT01084252

Phase 1/2 Dose Escalation and Efficacy Study of Anti-CD38 Monoclonal Antibody in Patients With Selected CD38+ Hematological Malignancies

NCT01084252

Phase 1/2 Completed 351 enrolled Sanofi
RandomizedParallel-groupOpen-labelTreatment

Summary

Primary Objective: Phase 1: To determine the maximum tolerated dose (MTD)/maximum administered dose (MAD) of SAR650984 (Isatuximab). Phase 2 (stage 1): To evaluate the activity of single-agent Isatuximab at different doses/schedules and to select dose and regimen to further evaluate the overall response rate (ORR) of Isatuximab as single agent or in combination with dexamethasone. Phase 2 (stage 2): To evaluate the activity in terms of overall response rate (ORR) of Isatuximab at the selected dose/schedule from stage1, as single agent (ISA arm) and in combination with dexamethasone (ISAdex arm). Secondary Objectives: Phase 1: * To characterize the global safety profile including cumulative toxicities. * To evaluate the pharmacokinetic (PK) profile of Isatuximab in the proposed dosing schedule(s). * To assess the pharmacodynamics (PD), immune response, and preliminary disease response. Phase 2 (stage 1): to evaluate the following objectives for Isatuximab as single agent: * Safety * Efficacy as measured by duration of response, clinical benefit rate, progression free survival, overall survival. Phase 2 (stage 2): to evaluate the following objectives in each arm (ISA and ISAdex): * Safety * Efficacy as measured by duration of response, clinical benefit rate, progression free survival, overall survival. * Participant-reported changes in health-related quality of life, symptoms of multiple myeloma and generic health status. * Pharmacokinetic profile of Isatuximab. * Immunogenicity of Isatuximab. * Investigate the relationship between CD38 receptor density and CD38 receptor occupancy (Stage 1 only) on multiple myeloma cells and parameters of clinical response.

Timeline

Start
2010-05-11
Primary completion
2018-12-21
Completion
2023-07-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Dexamethasone Small molecule 20 mg Intravenous
Subject Dexamethasone Small molecule 40 mg Intravenous
Subject Isatuximab Monoclonal antibody 0.0001 mg/kg Intravenous
Subject Isatuximab Monoclonal antibody 0.001 mg/kg Intravenous
Subject Isatuximab Monoclonal antibody 0.01 mg/kg Intravenous
Subject Isatuximab Monoclonal antibody 0.03 mg/kg Intravenous
Subject Isatuximab Monoclonal antibody 0.1 mg/kg Intravenous
Subject Isatuximab Monoclonal antibody 0.3 mg/kg Intravenous
Subject Isatuximab Monoclonal antibody 1 mg/kg Intravenous
Subject Isatuximab Monoclonal antibody 3 mg/kg Intravenous
Subject Isatuximab Monoclonal antibody 5 mg/kg Intravenous
Subject Isatuximab Monoclonal antibody 10 mg/kg Intravenous
Subject Isatuximab Monoclonal antibody 20 mg/kg Intravenous