This study was to find out if patients with Relapsing Remitting Multiple Sclerosis treated with Interferon beta-1a had an improved quality of life after treatment with Interferon beta-1a
The study was an open-label, multi-center, international post-marketing study (phase 4). Eligible patients were interferon naïve patients suffering from relapsing MS. The duration of a subject's participation in the study was up to a maximum 26 months.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
284
IM injection
Coordinating Research Site
Sijsele-Damme, Belgium
Coordinating Research Site
Esch-sur-Alzette, Luxembourg
Coordinating Research Site
Glasgow, Scotland, United Kingdom
The primary objective of this study is to evaluate the correlation between the MS Functional Composite Index and two Quality of Life scales (MS Quality of Life 54 and AMS Quality of Life) in patients treated with interferon beta-1a (AVONEX®).
Time frame: screening, Day -30, Day -1, Months 3, 6, 12, 18, and 24
Reproducibility of Quality of Life scales per language version
Time frame: months 18 and 24
Reliability of the Quality of Life scales per language version
Time frame: months 18 and 24
EDSS score throughout the study
Time frame: screening, Day -1, Months 12 and 24
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