Glyburide Advantage in Malignant Edema and Stroke Pilot
Status: | Archived |
---|---|
Conditions: | Peripheral Vascular Disease, Cardiology, Neurology |
Therapuetic Areas: | Cardiology / Vascular Diseases, Neurology |
Healthy: | No |
Age Range: | Any |
Updated: | 7/1/2011 |
Start Date: | March 2011 |
End Date: | December 2011 |
A Two-center, Prospective, Open Label, Phase IIa Trial of RP-1127 (Glyburide for Injection) in Patients With a Severe Anterior Circulation Ischemic Stroke Who Are Likely to Experience Clinically Significant Brain Swelling.
The study objective is to assess the feasibility of enrolling, evaluating, and treating with
RP-1127 (Glyburide for Injection) severe anterior circulation ischemic stroke patients,
whether or not treated with standard of care IV rtPA. Patients must be between 18-60 years
of age, must have a baseline diffusion weighted image (DWI) lesion volume 82 - 210 cm3, and
time from symptom onset to start of study infusion must be ≤10 hr.
This is a two-center, prospective, open label, Phase IIa trial of RP-1127 (Glyburide for
Injection) in 10 patients with a severe anterior circulation ischemic stroke who are likely
to experience clinically significant brain swelling.
Subjects will receive RP-1127 (Glyburide for Injection), delivered as an IV bolus followed
by an IV infusion for 72 hours.
Subjects will have a baseline (pretreatment) MRI scan as standard of care, and three fol-low
up MRI scans (at 24+12 hours, 48+12 hours, and 72±12 hours). Since recanalization may have
an effect on outcome, the results of vascular studies, obtained as part of stan-dard of care
and defined as CTA, MRA or catheter angiography of the head and neck, will be recorded. .
Additionally, clinical endpoints such as the NIHSS, GCS and FOUR Score (baseline, 24±12
hour, 48±12 hour, 72±12 hour and 7±1 days) and mRS (30±5 days and 90±7 days) will be
assessed. Safety parameters will be assessed through Day 7 or discharge (whichever is
sooner), and then again at Day 30±5 and Day 90±7.
Study participation is expected to last 90±7 days.
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