drugset / Trial / NCT01268683

Glyburide Advantage in Malignant Edema and Stroke Pilot

NCT01268683

NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this study is to assess the feasibility of enrolling, evaluating, and treating with glyburide for injection severe anterior circulation ischemic stroke participants, whether or not treated with standard of care intravenous (IV) recombinant tissue plasminogen activator (rtPA). Participants must be between 18-80 years of age, must have a baseline diffusion weighted image (DWI) lesion volume 82 -210 centimeters cubed (cm3), and time from symptom onset to start of study infusion must be ≤10 hour(hr). The secondary objectives are to assess the initial safety and tolerability, and pharmacokinetics (PK) /pharmacodynamics (PD) of glyburide in severe stroke participants, as well as to compare the clinical and magnetic resonance imaging (MRI) outcome data to benchmark data derived from published literature.

Timeline

Start
2011-05-26
Primary completion
2012-06-07
Completion
2012-06-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Glyburide Small molecule 3 mg Intravenous

Indications