Trial Profile

Open-label, Single-blinded, Observational, Prospective, 24-months, Longitudinal, Controlled Study to Assess the Efficacy of Gilenya® on Development of Thalamus Pathology and Cognitive Impairment in Patients With Relapsing Forms of Multiple Sclerosis.

Status: Completed

Phase of Trial: Phase IV

Latest Information Update: 18 Apr 2019

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At a glance

15 Apr 2019 Status changed from active, no longer recruiting to completed.
01 May 2017 Planned End Date changed from 1 Jan 2017 to 1 Oct 2018.
01 May 2017 Planned primary completion date changed from 1 Oct 2016 to 1 Sep 2018.

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