Observational Study of Tysabri in Early Relapsing-Remitting Multiple Sclerosis in Anti-JC Virus Antibody Negative Participants
Completed
Conditions studied: Relapsing-Remitting Multiple Sclerosis
In brief
The primary objective of the study is to determine which baseline and yearly response factors (clinical and para clinical) predict overall disease-free status at Month 12 and Month 24, and clinical disease-free status in subsequent Months 36 and 48. The secondary objectives are: To identify prognostic factors at Baseline that predict overall disease-free status at Month 12, and to assess if yearly overall disease-free response factors predict overall disease-free status at Month 24; To evaluate clinical disease-free status (relapse, Expanded Disability Status Scale \[EDSS\]) at each analysis time point of Months 12, 24, 36, and 48; To identify prognostic factors at Baseline that predict clinical disease-free status at Month 12, and to assess yearly clinical disease-free response factors that predict clinical disease-free status (relapse, EDSS) in subsequent years at Months 24, 36, and 48; To evaluate the impact of Tysabri at each analysis time point of Months 12, 24, 36, and 48 on the following: annualized relapse rate (ARR), sustained EDSS progression and improvement (24-week sustained); To evaluate the impact of Tysabri at each analysis time point of Months 12, 24, 36, and 48 on the following: magnetic resonance image (MRI) measures: T2, T1, T1 with Gadolinium (Gd), brain atrophy; To evaluate the impact of Tysabri at Month 24 and Month 48 on the following: optical coherence tomography (OCT), Low and High Contrast Visual Acuity Assessment; To evaluate the impact of Tysabri at each analysis time point of Months 12, 24, 36, and 48 on the following: cognitive impairment (Symbol Digit Modalities Test \[SDMT\]), capacity for work (Work Productivity and Activity Impairment Questionnaire \[WPAI\]), quality of life (QoL) (Multiple Sclerosis Impact Scale \[MSIS-29\])
Key facts
- Study ID
- NCT01485003
- Run by
- Biogen
- People needed
- 231
- Starts
- 2012-02-07
- Expected to finish
- 2018-11-26
- Last updated by the study team
- 2019-02-12
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Research Site — Homewood, Alabama, United States
- Research Site — Sun City, Arizona, United States
- Research Site — La Jolla, California, United States
- Research Site — Los Angeles, California, United States
- Research Site — Aurora, Colorado, United States
- Research Site — Fort Collins, Colorado, United States
- Research Site — Newark, Delaware, United States
- Research Site — Washington D.C., District of Columbia, United States
- Research Site — Jacksonville, Florida, United States
- Research Site — Atlanta, Georgia, United States
- Research Site — Chicago, Illinois, United States
- Research Site — Lake Barrington, Illinois, United States
- Research Site — Peoria, Illinois, United States
- Research Site — Indianapolis, Indiana, United States
- Research Site — Indianapolis, Indiana, United States
- Research Site — Overland Park, Kansas, United States
- Research Site — Louisville, Kentucky, United States
- Research Site — New Orleans, Louisiana, United States
- Research Site — Baltimore, Maryland, United States
- Research Site — Boston, Massachusetts, United States
- Research Site — Lexington, Massachusetts, United States
- Research Site — Wellesley Hills, Massachusetts, United States
- Research Site — Worcester, Massachusetts, United States
- Research Site — East Lansing, Michigan, United States
- Research Site — Lincoln, Nebraska, United States
Full record on ClinicalTrials.gov
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