Efficacy and Safety of LT3001 on Treating the Acute Ischemic Stroke

Ki vehet részt

• Subjects aged between 18 and 80 years at screening
• Clinical diagnosis of acute ischemic stroke that causes evaluable neurological impairment; 3.4 points ≤ NIHSS score ≤ 25 points at randomization; 4.Subjects who are able to receive the investigational drug within 24 hours after the onset of stroke; 5.Female subjects of childbearing potential or male subjects whose sexual partner are women of childbearing potential have no pregnancy plan and voluntarily take effective contraceptive measures during the study period and for 3 months after the last dose; 6.All subjects sign the informed consent form by themselves or their guardians after receiving complete study information

Ki nem vehet részt

• Subjects have received or plan to receive endovascular treatment and/or intravenous thrombolytic therapy recommended by Chinese Guidelines for Diagnosis and Treatment of Acute Ischemic Stroke 2018 during this onset period
• Subjects who have used or are using protocol-prohibited medications after the onset
• Patients who are unable to cooperate due to epileptic seizure at the onset of stroke or other concomitant mental disorders or are unwilling to cooperate
• Systolic blood pressure > 180 mmHg and/or diastolic blood pressure > 100 mmHg after active antihypertensive therapy
• Subjects who underwent any major surgery before screening
• Subjects who have participated in another investigational study and used investigational product before screening
• Subjects with pre-stroke disability
• Subjects with intracranial hemorrhagic diseases, tumor in brain parenchyma, arteriovenous malformation, aortic arch dissection, other central nervous system lesions that may increase the risk of hemorrhage, or imaging evidence for arterial aneurysm requiring treatment
• Acute hemorrhage tendency
• Active visceral hemorrhage
• Subjects with a history of serious hypersensitivity
• Subjects who experienced AIS, ICH, acute myocardial infarction or serious head trauma before screening
• Subjects with a history of active digestive ulcer before screening
• Subjects who experienced hemorrhagic disease before screening
• Serious hepatic impairment or serious renal insufficiency
• Other conditions unsuitable for participation in this study determined by the Investigator
• Blood glucose level < 50 mg/dL or > 400 mg/dL
• Presence of disturbances of consciousness at screening and NIHSS 1a ≥ 2 points
• Neurological signs have improved rapidly and spontaneously at screening
• Massive infarction on imaging
• Lactating or pregnant subjects, or women of childbearing potential with positive pregnancy test results
• International normalized ratio > 1.7 or prothrombin time > 15 s
• Subjects who underwent arterial puncture at the site not easy for hemostasis by compression before screening