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| Sponsor: | Mitsubishi Tanabe Pharma Corporation |
|---|---|
| Collaborator: |
Kyowa Hakko Kogyo Co., Ltd. |
| Information provided by: | Mitsubishi Tanabe Pharma Corporation |
| ClinicalTrials.gov Identifier: | NCT00147316 |
Purpose
Based on previous studies comparing different rt-PA doses, we performed a clinical trial with 0.6mg/kg, which is lower than the internationally approved dosage of 0.9mg/kg, aiming to assess the efficacy and safety of alteplase for the Japanese.
| Condition | Intervention | Phase |
|---|---|---|
|
Cerebral Infarction Brain Ischemia |
Drug: alteplase |
Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Non-Randomized, Open Label, Historical Control, Single Group Assignment, Safety/Efficacy Study |
| Official Title: | Japan Alteplase Clinical Trial(J-ACT): Phase 3 Efficacy and Safety Study of Tissue Plasminogen Activator for Acute Ischemic Stroke Within 3 Hours of Onset |
| Estimated Enrollment: | 100 |
| Study Start Date: | April 2002 |
| Estimated Study Completion Date: | September 2003 |
Based on previous studies comparing different rt-PA doses, we performed a clinical trial with 0.6mg/kg, which is lower than the internationally approved dosage of 0.9mg/kg, aiming to assess the efficacy and safety of alteplase for the Japanese.
The primary endpoints were the rate of patients with a modified Rankin Scale (mRS) score of 0-1 at 3 months and the incidence of symptomatic intracranial hemorrhage (sICH) within 36 hours. Thresholds for these endpoints were determined by calculating 90% confidence intervals of weighted averages derived from published reports. The protocol was defined according to the National Institute of Neurological Disorders and Stroke (NINDS) rt-PA stroke study with slight modifications.
Eligibility| Ages Eligible for Study: | 20 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Patients with acute ischemic stroke within 3 hours of onset, with a clearly defined time of onset
Exclusion Criteria:
Contacts and Locations| Japan, Osaka | |
| National Cardiovascular Center | |
| Suita, Osaka, Japan, 565-8565 | |
| Study Chair: | Takenori Yamaguchi, MD | National Cardiovascular Center |
More Information
| Study ID Numbers: | 527-0110 |
| Study First Received: | September 5, 2005 |
| Last Updated: | September 5, 2005 |
| ClinicalTrials.gov Identifier: | NCT00147316 History of Changes |
| Health Authority: | Japan: Ministry of Health, Labor and Welfare |
|
acute stroke thrombolytic therapy tissue plasminogen activator |
|
Molecular Mechanisms of Pharmacological Action Cerebral Infarction Hematologic Agents Stroke Nervous System Diseases Vascular Diseases Tissue Plasminogen Activator Central Nervous System Diseases Fibrinolytic Agents Cardiovascular Agents Ischemia Brain Diseases |
Cerebrovascular Disorders Pharmacologic Actions Fibrin Modulating Agents Necrosis Pathologic Processes Therapeutic Uses Brain Ischemia Cardiovascular Diseases Brain Infarction Infarction Plasminogen |