Overview

A Single Ascending Dose Study of GZ402668 in Patients With Progressive Multiple Sclerosis

Status:
Completed
Trial end date:
2018-05-16
Target enrollment:
Participant gender:
Summary
Primary Objective: To assess the safety and tolerability of GZ402668 after a single subcutaneous (SC) dose in men and women with progressive multiple sclerosis. Secondary Objectives: To assess in men and women with progressive multiple sclerosis: - The pharmacokinetic (PK) parameters of GZ402668 after a single SC dose. - The pharmacodynamic (PD) response to GZ402668 after a single SC dose.
Phase:
Phase 1
Details
Lead Sponsor:
Sanofi
Treatments:
Acyclovir