Efficacy and Safety of LT3001 on Treating the Acute Ischemic Stroke
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: LT3001 Drug:high dose, Placebo, LT3001 Drug:low dose.
- Who it may be relevant to
- Registry conditions: Acute Ischemic Stroke. Basic parameters: 18 years — 80 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
A Phase II Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Clinical Study to Evaluate the Safety and Efficacy of LT3001 in Subjects With Acute Ischemic Stroke (AIS)
Overview
This phase II clinical study is designed to evaluate the safety and efficacy of LT3001 in the treatment of acute ischemic stroke
Interventions
- Drug LT3001 Drug:high dose
Administered by intravenous infusion. - Drug Placebo
Administered by intravenous infusion. - Drug LT3001 Drug:low dose
Administered by intravenous infusion.
Primary outcome measures
- Incidence Adverse Events [Time frame: Approximately 2 years]
Secondary outcome measures (4)
- Proportion of subjects by mRS（Modified Rankin Scale） score (0 - 2) [Time frame: Day 30 and Day 90 after the first dose]
- Proportion of subjects with an NIHSS（National Institute of Health stroke scale ） score of ≤ 1 point and/or with a decrease of ≥ 4 points from baseline in NIHSS score [Time frame: Day 14 after the first dose]
- Absolute change from baseline in NIHSS score [Time frame: Day 3、Day 7、Day 14 and Day 30 after the first dose]
- Proportion of subjects with a BI（Barthel index） score of ≥ 95 points and ≥ 75 points [Time frame: Day 30 and Day 90 after the first dose]
Eligibility criteria
Inclusion criteria
- 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.
Exclusion criteria
- 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;
- Presence of disturbances of consciousness at screening and NIHSS 1a ≥ 2 points;
- Neurological signs have improved rapidly and spontaneously at screening;
- Subjects who have used or are using protocol-prohibited medications after the onset;
- 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;
- Massive infarction on imaging;
- 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;
- Acute hemorrhage tendency;
- Blood glucose level < 50 mg/dL or > 400 mg/dL;
- Active visceral hemorrhage;
- 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 with a history of serious hypersensitivity;
- Subjects who experienced AIS, ICH, acute myocardial infarction or serious head trauma before screening;
- Subjects who underwent any major surgery before screening;
- Subjects with a history of active digestive ulcer before screening;
- Subjects who experienced hemorrhagic disease before screening;
- Subjects who underwent arterial puncture at the site not easy for hemostasis by compression before screening;
- Serious hepatic impairment or serious renal insufficiency;
- Subjects who have participated in another investigational study and used investigational product before screening;
- Other conditions unsuitable for participation in this study determined by the Investigator.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Treatment
Study locations
China · 28 centers
- Beijing Luhe Hospital Capital Medical University — Beijing
- The First Affiliated Hospital of Jinan University — Guangzhou
- Luoyang Third People's Hospital — Luoyang
- Harrison International Peace Hospital — Hengshui
- Daqing Oilfield General Hospital — Daqing
- Zhongnan Hospital of Wuhan University — Wuhan
- The First Affiliated Hospital of Baotou Medical College — Baotou
- Inner Mongolia Baogang Hospital — Baotou
- … and 20 more centers
Identifiers
NCT: NCT05686642 · SPH-LT3001-202