drugset / Trial / NCT00401310

The Efficacy and Safety of MK0724 IV for Improvement of Neurological Damage and Recovery From Middle Cerebral Artery Ischemic Stroke (0724-018)

NCT00401310 ↗

Phase 2 Terminated 150 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

The safety and efficacy of MK0724 will be assessed in patients with acute middle cerebral artery stroke using the Action Reach Arm Test (ARAT). This test allows measurement of a specific functional deficit and subsequent recovery correlating with the specific area of stroke in the brain.

Timeline

Start
2007-07
Primary completion
2009-01
Completion
2009-01

Outcome

Outcome not reported

Stopped: “Termination date was 20-Oct-2008. Subjects were monitored during the post treatment 90 day follow-up period (per protocol) resulting in LPLV 19-Jan-2009.”

Drugs

EvaluationDrugModalityDoseRoute
Subject ARUNDIC ACID Small molecule 8 mg/kg Intravenous