Clinical trial

Study to Evaluate Safety, Tolerability, and Effect of AL208 on Mild Cognitive…

NCT00404014 · Allon Therapeutics, Industry · Completed

Key facts

NCT number NCT00404014
Title Study to Evaluate Safety, Tolerability, and Effect of AL208 on Mild Cognitive Impairment Following Coronary Artery Bypass Graft Surgery
Official title A Phase II Study Designed to Evaluate the Safety, Tolerability, and Effect of a Single, Rising Dose of Intravenous AL-208, Followed by a Placebo-Controlled, Double-Blind, Parallel-Group Evaluation of a Single Dose of AL-208, on Mild Cognitive Impairment Following Coronary Artery Bypass Graft…
Lead sponsor Allon Therapeutics, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Mild Cognitive Impairment
Intervention type Drug
Interventions AL-208, Placebo
Enrollment 234
Start date Aug 1, 2006
Primary completion Jun 1, 2008
Completion Jun 1, 2008
First posted Nov 27, 2006
Last update posted Oct 24, 2012
Countries Canada, United States

At a glance

  • 10–99 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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