A Study to Evaluate the Effects of ONO-2506 Intravenous Infusion in Patients With Acute Ischemic Stroke | NCT00046761 | Trialant

A Study to Evaluate the Effects of ONO-2506 Intravenous Infusion in Patients With Acute Ischemic Stroke | NCT00046761 | Trialant

Ages Eligible for Study: Adult (18-64)Older Adult (65+)
Sexes Eligible for Study: All
Accepts Healthy Volunteers: No
Eligibility Criteria: Inclusion Criteria:

Patient must have a clinical diagnosis of acute cortical ischemic stroke.

Patient must be randomized into the study within six hours after the initial onset of stroke symptoms.

Patient must have a measurable focal neurological deficit for a minimum duration of 60 minutes.

Patient must have a CT or MRI examination compatible with the clinical diagnosis of acute ischemic stroke.

Patient must have had a pre-stroke mRS scale score of 0 or 1.

Other inclusion criteria as specified in the study protocol.

Exclusion Criteria:

Patient must not have a body weight of more than 125 kg.

Patient must not have a CT and/or MRI with evidence of a non-ischemic mechanism, subarachnoid hemorrhage, or primary intracerebral and/or intraventricular hemorrhage.

Patient must not have all three of the following findings:

reduced level of consciousness (has score of greater than or equal to two on NIHSS Question 1a)

forced eye deviation or total gaze paresis (has score of 2 on NIHSS Question 2) and

dense hemiplegia (no movement) of upper and lower extremities (i.e., has score of 4 on NIHSS Question 5 regarding motor arm and has score of 4 on NIHSS Question 6 regarding motor leg).

Patient must not have neurological signs and symptoms that are rapidly improving.

Patient must not have a severe coexisting or terminal systemic disease.

Patient must not be pregnant or lactating.

Patient must not have impaired hepatic function; bilirubin greater than 2 mg/dL and or ascites.

Patient must not have impaired renal function; serum creatinine greater than 2 mg/dL.

Patient must not have congestive heart failure.

Patient must not have a baseline ECG showing a PR interval greater than 200 milliseconds, or a corrected QT interval of greater than 480 milliseconds, or a history of ventricular arrhythmias, or a Mobitz Type 1 or greater AV block.

Patient must not have other exclusion criteria as specified in the study protocol.