TNK-tPA
DrugExperimental arms for low, middle, and high dosing; and active control arm for the standard protocol
Other names: rtPA
NCT Number: NCT04676659
To explore the safe and efficacious dose of rhTNK-tPA injection administered within 3 hours after onset of hyperacute ischemic stroke; to provide dose evidence for phase III clinical trial.
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Notify Me18 year and older
All sexes
Interventional
Phase 2
Beijing Tiantan Hospital, Capital Medical University, Beijing, Beijing Municipality, China
To evaluate the safety and efficacy of rhTNK-tPA at different doses of 0.10 mg/kg, 0.25 mg/kg and 0.32 mg/kg compared with standard rt-PA intravenous thrombolytic therapy within 3 hours after onset of ischemic stroke. The primary objective of this study is to evaluate the differences of NIHSS scores among the four treatment groups at 14 days after intravenous thrombolysis.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
1.1 History of severe head trauma or stroke within 3 months; 1.2 Suspected subarachnoid hemorrhage; 1.3 Arterial puncture at a non-compressible site within the previous 1week; 1.4 History of intracranial hemorrhage; 1.5 Intracranial tumor, vascular malformation, or arterial aneurysm; 1.6 Recent intracranial or intraspinal surgery; 1.7 Systolic blood pressure ≧ 180 mm Hg, or diastolic blood pressure ≧ 100 mm Hg; Increased blood pressure; 1.8 Active internal bleeding ; 1.9 Acute bleeding tendency, including platelet count below 100×109/L or otherwise; 1.10 Heparin treatment was performed within 48 h ( APTT exceeded the upper limit of normal range ) ; 1.11 Warfarin has been taken orally , and the international standardized ratio is INR > 1.7 or PT > 15 s ; 1.12 Anticoagulant drugs such as thrombin inhibitor or Xa factor inhibitor , argatroban ( including new anticoagulants with unclear mechanism ) are currently being used , and various sensitive laboratory tests are abnormal ( such as live ) APTT , INR , Platelet count , Serpentine ECT of pulse enzyme setting time ; thrombin time TT or appropriate determination of Xa factor activity ) ; 1.13 Blood glucose < 2.7 mmol/L; 1.14 CT showed multilobular infarction ( low density > 1 / 3 cerebral hemisphere )
2.1 Mild stroke or stroke with rapid improvement of symptoms; 2.2 Women in pregnancy ; 2.3 Symptoms of neurological impairment after seizures ; 2.4 There have been major surgical operations or serious injuries in the last 2 weeks; 2.5 There were gastrointestinal or urinary system bleeding in recent 3 weeks ; 2.6 History of myocardial infarction within 3 months.
Experimental arms for low, middle, and high dosing; and active control arm for the standard protocol
Other names: rtPA
Time frame: 14 days
Proportion of subjects with NIHSS 1 or at least 4 on the NIHSS score decreased from the baseline at day14.
Time frame: 90 days
Time frame: 90 days
Neurological impairment defined as change of NIHSS score at 90 days.
Time frame: 90 days
Global function of daily living defined as BI ≥ 95 at 90 days.
Time frame: 90 days
Quality of life measured by EQ-5D scale.
Time frame: 36 hours
Proportion of subjects with symptomatic intracranial hemorrhage (sICH) at 36 hours.
Time frame: 90 days
Overall mortality rate at 90 days.
Time frame: 90 days
Proportion of patients with asymptomatic intracranial hemorrhage at 90 days.
Time frame: 90 days
The proportion of patients with other bleeding events was defined by GUSTO bleeding at 90 days.
Time frame: 90 days
Proportion of patients with adverse events / severe adverse events at 90 days.
Beijing Tiantan Hospital
Other
Phase II Dose-finding Open Study of Recombinant Human TNK Tissue-type Plasminogen Activator (rhTNK-tPA) Injection Administered Within 3 Hours After Onset of Hyperacute Ischemic Stroke
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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