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A Phase I, Double-blind, Randomized, Placebo-controlled, Parallel-group Study to Assess the Safety, Tolerability and Pharmacokinetics of Oral AZD5213 After Administration of Multiple Ascending Doses for 10 Days in Healthy Male and Non-fertile Female Volunteers.

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A Phase I, Double-blind, Randomized, Placebo-controlled, Parallel-group Study to Assess the Safety, Tolerability and Pharmacokinetics of Oral AZD5213 After Administration of Multiple Ascending Doses for 10 Days in Healthy Male and Non-fertile Female Volunteers.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 04 Feb 2015

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At a glance

  • Drugs AZD 5213 (Primary)
  • Indications Alzheimer's disease; Attention-deficit hyperactivity disorder
  • Focus Adverse reactions
  • Sponsors AstraZeneca

    • Most Recent Events

    • 12 Jul 2011 Actual end date (May 2011) added as reported by ClinicalTrials.gov.
    • 12 Jul 2011 Status changed from recruiting to completed as reported by ClinicalTrials.gov.
    • 07 Dec 2010 Planned end date changed from 1 Sep 2010 to 1 Feb 2011 as reported by ClinicalTrials.gov.

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