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Clinical trial

A Dose Escalation, Safety, Pharmacokinetic, Pharmacodynamic and Preliminary Efficacy Study of SAR650984 (Isatuximab) Administered Intravenously in Combination With Bortezomib - Based Regimens in Adult Patients With Newly Diagnosed Multiple Myeloma Non Eligible for Transplantation or No Intent for Immediate Transplantation

NCT02513186 is registered in ClinicalTrials.gov with Sanofi as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Dose Escalation, Safety, Pharmacokinetic, Pharmacodynamic and Preliminary Efficacy Study of SAR650984 (Isatuximab) Administered Intravenously in Combination With Bortezomib - Based Regimens in Adult Patients With Newly Diagnosed Multiple Myeloma Non Eligible for Transplantation or No Intent for Immediate Transplantation
Lead sponsor
Sanofi
Phase
Phase 1
Overall status
Completed
Start date
September 30, 2015
Completion date
January 22, 2024
Enrollment
90 (actual)
Sites
12

Conditions

As the registry lists them; a condition with its own page is linked.

plasma cell myeloma