drugset / Trial / NCT00725985

Oral Cladribine in Early Multiple Sclerosis (MS)

NCT00725985

Phase 3 Completed 617 enrolled EMD Serono Research & Development Institute, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A randomized, double-blind, clinical trial to assess the safety and efficacy of two doses of oral cladribine versus placebo in participants who had a first clinical demyelinating event (clinically isolated syndrome). Participants in either the cladribine or placebo group may also enter treatment periods with open-label interferon-beta or open-label cladribine depending upon the disease status. The primary objective of this study is to evaluate the effect of two dosage regimens of oral cladribine versus placebo on the time to conversion to multiple sclerosis (MS) (from randomization) according to the Poser criteria in participants with first clinical demyelinating event at high risk of converting to MS.

Timeline

Start
2008-12-31
Primary completion
2011-07-31
Completion
2012-04-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Cladribine Small molecule 3.5 mg/kg Oral
Subject Cladribine Small molecule 5.25 mg/kg Oral
Background Interferon beta-1a Protein / enzyme biologic 44 ug Subcutaneous

Indications