Clinical Trials Directory

Trials / Completed

CompletedNCT01074346

Tolerability of Rebif® (Interferon-beta 1-A) Therapy in Korean Patients With Multiple Sclerosis

A Prospective, Multi-center, Observational Study to Assess the Tolerability of Interferon-beta 1-A (Rebif®) Therapy for Korean Patients With Multiple Sclerosis

Status
Completed
Phase
Study type
Observational
Enrollment
60 (actual)
Sponsor
Merck KGaA, Darmstadt, Germany · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

This is an observational study to assess the tolerability of Rebif treatment in Korean multiple sclerosis (MS) subjects.

Detailed description

The present observational study is being conducted to assess the safety information from a target of 100 Korean subjects with MS treated with Rebif. Various parameters like subjects' background (age, sex, BMI), MS history, MS status (MS type, Expanded Disability Status Score \[EDSS\] and others), MS Treatment Concern Questionnaire (MSTCQ), Rebif treatment status, concomitant disease modifying agents (DMA) therapy and Rebif related adverse events will be collected. Subjects will be followed for 12 months. Proportion of subjects with moderate to severe (Grade 3-5) injection site reactions after 3, 6, 12 months of Rebif treatment will be determined. Secondary outcomes like annual relapse rate, change in EDSS, changes in MSTCQ, time to first relapse and incidence of side effects associated with Rebif therapy will also be determined and presented descriptively. OBJECTIVES Primary objectives * To assess the tolerability of Rebif treatment in Korean MS subjects in a non-interventional setting Secondary Objectives * To evaluate subject's satisfaction, clinical data and disease characteristics of the population of MS subjects undergoing Rebif treatment.

Conditions

Interventions

TypeNameDescription
DRUGInterferon-β-1aInterferon-β-1a according to the standard practice

Timeline

Start date
2008-08-01
Primary completion
2011-11-01
Completion
2011-11-01
First posted
2010-02-24
Last updated
2014-02-19

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01074346. Inclusion in this directory is not an endorsement.