A Randomized, Placebo-Controlled, Multicenter Study to Evaluate the Safety and Tolerability of Multiple Dose Regimens of CHF 5074 (200, 400, 600 mg/Day for up to 12 Weeks) and to Explore the Effects on Potential Markers of Clinical Efficacy in Patients With Mild Cognitive Impairment

Trial Profile

A Randomized, Placebo-Controlled, Multicenter Study to Evaluate the Safety and Tolerability of Multiple Dose Regimens of CHF 5074 (200, 400, 600 mg/Day for up to 12 Weeks) and to Explore the Effects on Potential Markers of Clinical Efficacy in Patients With Mild Cognitive Impairment

Completed
Phase of Trial: Phase II

Latest Information Update: 03 Feb 2016

At a glance

  • Drugs CHF 5074 (Primary)
  • Indications Mild cognitive impairment
  • Focus Adverse reactions
  • Sponsors Chiesi; Chiesi Farmaceutici SpA
  • Most Recent Events

    • 07 Jun 2017 Biomarkers information updated
    • 08 Jan 2016 Primary endpoints has been revised according to ClinicalTrials.gov record.
    • 26 Jul 2013 Interim data from the 90-week open-label extension study have been reported, according to a Chiesi Farmaceutici S.p.A. and CereSpir media release; 43 patients are expected to reach the 90-week endpoint at the end of 2013.
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