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Clinical Trial Summary

The purpose of this study was to evaluate the improvement in spontaneous recovery from clinical deficits at the time of an acute relapse in RR-MS participants already receiving interferon (IFN) beta 1a with D-aspartate (versus placebo) as add-on therapy.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03387046
Study type Interventional
Source Merck KGaA, Darmstadt, Germany
Contact
Status Terminated
Phase Phase 2
Start date March 26, 2018
Completion date January 11, 2019

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