drugset / Trial / NCT00436826

A Phase 2 Study of Cladribine Add-on to Interferon-beta (IFN-beta) Therapy in Multiple Sclerosis (MS) Subjects With Active Disease (ONWARD)

NCT00436826

Phase 2 Completed 172 enrolled EMD Serono Research & Development Institute, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

The goal of this study was to evaluate the safety, tolerability and effectiveness of oral cladribine when taken in combination with Interferon-beta (IFN-beta) therapy for the treatment of multiple sclerosis (MS). This study randomized around 200 participants from approximately 50 sites located world-wide, who have experienced at least one relapse while taking IFN-beta therapy within 48 weeks prior to Screening, irrespective of disability progression. Secondary progressive multiple sclerosis (SPMS) participants, who were still experiencing relapses, and participants who have received disease modifying drugs (DMDs), other than IFN-beta therapy, during their MS treatment history, but were currently on IFN-beta therapy and have experienced active MS symptoms (at least 1 relapse) during the 48 weeks prior to Screening, were enrolled. Participants were randomized in a 2:1 fashion to receive up to 4 cycles of oral cladribine or matching placebo in combination with IFN-beta therapy. Participants who completed the double-blind portion of the study were invited to participate in an open-label extension phase of matching study design.

Timeline

Start
2006-11-30
Primary completion
2011-09-30
Completion
2012-03-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Cladribine Small molecule 3.5 mg/kg Oral
Background Interferon beta-1a Protein / enzyme biologic 30 ug Intramuscular
Background Interferon beta-1a Protein / enzyme biologic 44 ug Subcutaneous
Background Interferon beta-1b Protein / enzyme biologic 250 ug Subcutaneous

Indications