drugset / Trial / NCT00404014

Study to Evaluate Safety, Tolerability, and Effect of AL208 on Mild Cognitive Impairment Following Coronary Artery Bypass Graft Surgery

NCT00404014 ↗

Phase 2 Completed 234 enrolled Allon Therapeutics
RandomizedCrossoverQuadruple-blindTreatment

Summary

The primary objective is to compare mild cognitive impairment in the AL-208 group with the placebo group at 14 + - 3 days after CABG surgery

Timeline

Start
2006-08
Primary completion
2008-06
Completion
2008-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator davunetide Protein / enzyme biologic 300 mg Intravenous