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A Multinational, Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Followed by an Active Treatment Period, to Evaluate the Efficacy, Safety and Tolerability of Two Doses of Oral Administration of Laquinimod (0.6 mg/Day or 1.2 mg/Day) in Patients With Relapsing Remitting Multiple Sclerosis (RRMS)

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Trial Profile

A Multinational, Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Followed by an Active Treatment Period, to Evaluate the Efficacy, Safety and Tolerability of Two Doses of Oral Administration of Laquinimod (0.6 mg/Day or 1.2 mg/Day) in Patients With Relapsing Remitting Multiple Sclerosis (RRMS)

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 26 Apr 2022

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At a glance

  • Drugs Laquinimod (Primary)
  • Indications Multiple sclerosis
  • Focus Registrational; Therapeutic Use
  • Acronyms CONCERTO
  • Sponsors Teva Branded Pharmaceutical Products R&D; Teva Pharmaceutical Industries

    • Most Recent Events

    • 01 Apr 2022 Results published in the Multiple Sclerosis Journal
    • 02 Jul 2019 This trial has been discontinued in Germany, Italy, Poland, Spain, Greece, Austria, UK, Latvia, Slovakia, Bulgaria, Hungary, Estonia (End date: 2017-05-09), according to European Clinical Trials Database record.
    • 31 May 2017 This trial has been suspended in Germany as per European Clinical Trials Database record.

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