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A Randomized, Double-Blind, Placebo-Controlled Study to Determine Safety and Tolerability of LX6171 Oral Suspension Dosed for 28 Days in Subjects Exhibiting Age Associated Memory Impairment (AAMI) with a Lead-in, Open-Label, Single-Dose Relative Bioavailability Study of LX6171 Oral Suspension in Healthy Elderly Subjects.

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Trial Profile

A Randomized, Double-Blind, Placebo-Controlled Study to Determine Safety and Tolerability of LX6171 Oral Suspension Dosed for 28 Days in Subjects Exhibiting Age Associated Memory Impairment (AAMI) with a Lead-in, Open-Label, Single-Dose Relative Bioavailability Study of LX6171 Oral Suspension in Healthy Elderly Subjects.

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 02 Apr 2012

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At a glance

  • Drugs LX 6171 (Primary)
  • Indications Memory disorders
  • Focus Adverse reactions; Pharmacokinetics; Therapeutic Use
  • Sponsors Lexicon Pharmaceuticals
  • Most Recent Events

    • 02 Apr 2012 Inclusion and exclusion criteria amended as reported by European Clinical Trials Database record.
    • 24 Mar 2012 Primary endpoints identified as reported by European Clinical Trials Database record.
    • 24 Mar 2012 Planned number of patients changed from 120 to 136 as reported by European Clinical Trials Database record.
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