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Clinical Trial Summary

The main objectives of Part 1 are as follows: To evaluate the safety, tolerability, and efficacy of BG00012 in pediatric subjects with RRMS, as compared with a disease-modifying treatment and to assess health outcomes and evolution of disability. The primary objective of Part 2 is to evaluate the long-term safety of BG00012 in subjects who completed Week 96 in Part 1 of Study 109MS306. The secondary objective of Part 2 is to describe the long-term MS outcomes of BG00012 in subjects who completed Week 96 in Part 1 of Study 109MS306.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02283853
Study type Interventional
Source Biogen
Contact
Status Active, not recruiting
Phase Phase 3
Start date August 28, 2014
Completion date September 8, 2025

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