A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group, Dose-range-finding Study to Evaluate the Efficacy and Safety of TF0023 Spray Versus Placebo in Functional Improvement of Patients With Ischemic Strokes
试验速览
- 阶段
- 2 期
- 状态
- 暂停
- 入组人数
- 225
- 试验地点
- 24
- 主要终点
- The primary efficacy endpoint is the change from baseline in the mRS score for all randomized patients at Week 16 in Part A and Part B.
研究概览
简要总结
This is a phase 2, multicenter, randomized, double-blind (within dose), placebo controlled, parallel-group, dose-range finding study to evaluate the efficacy and safety of TF0023 spray versus placebo in functional improvement of patients with ischemic strokes under standard of care.
详细描述
This randomized, double-blind (within dose), placebo-controlled, parallel group study will be conducted in 2 parts to evaluate the efficacy and safety of TF0023 spray versus placebo in functional improvement in patients with ischemic strokes. Part A will evaluate the safety and efficacy of TF0023 spray in a higher dose . Efficacy will be assessed by the change in modified Rankin Scale (mRS) score from baseline to Week 16. At Week 16, a blinded interim analysis will be performed to determine if TF0023 shows positive results with a higher proportion of patients in the TF0023 group showing a more favorable outcome compared with the placebo group. If the results are positive, then Part B will be initiated to further evaluate safety and efficacy of TF0023 spray as well as to determine the best dosing regimen for the signs and symptoms and functional improvement of patients with ischemic strokes.
Part A In Part A , approximately 200 patients who are stable per the NIHSS will be screened as early as 3 days (72 hours) after the onset of stroke symptoms and approximately 75 will be randomized to active or placebo treatment in a 2:1 ratio (TF0023 [50 patients] and placebo [25 patients]).
Each patient enrolled in Group A will receive study treatment in a double-blind manner for 16 weeks starting between 3 and 60 days after the onset of stroke symptoms (Day 1 of the study). Qualified study personnel will instruct the patients and/or caregivers how to apply the study treatment accurately so that patients or caregivers will administer high dose of either TF0023 or placebo twice daily (approximately every 12 hours).
Patients will return to the study site at Weeks 4, 8, 12, and 16 for efficacy and safety assessments. After the Week 16 assessments have been performed, patients will receive active treatment in an open-label manner starting the next day through the end of the study (EOS) at Week 32. Patients will return to the study site at Week 24 and Week 32 (EOS) for efficacy and safety assessments. An Early Termination visit will occur if the patient is discontinued from the study prematurely. Patients will have a follow-up visit approximately 14 days after the Early Termination visit or the Week 32 (EOS) visit.
An interim analysis will be performed using the data collected through the study up to and including the Week 16 visit. If the analysis of the mRS shows that treatment with TF0023 is positive compared with placebo (mRS score of 0 to 2 indicates functional independence), Part B will start to enroll patients. If the analysis shows that treatment with TF0023 is not positive compared with placebo (mRS score >2), Part B will not enroll any patients.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Care Provider, Investigator)
入排标准
- 年龄范围
- 18 Years 至 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female 18 to 85 years of age at the time of signing the informed consent form.
- •Patient or patient's legal representative must understand and voluntarily sign the informed consent form prior to any study-related assessments/procedures are conducted.
- •Able to adhere to the study visit schedule and other protocol requirements.
- •A female of childbearing potential must have a negative serum at screening and negative urine pregnancy test prior to treatment with study therapy. In addition, sexually active females of childbearing potential must agree to use two of the following adequate forms of contraception methods simultaneously: oral, injectable or implantable hormonal contraception; tubal ligation; intrauterine device; barrier contraceptive with spermicide; or vasectomized partner for the duration of the study and the follow-up period. Males, including those who have had a vasectomy, must agree to use barrier contraception (latex condoms) when engaging in reproductive sexual activity with a female of childbearing potential for the duration of study and follow-up period.
- •Must have a diagnosis of ischemic stroke and be stable enough to be randomized to treatment within 3 to 60 days after the onset of stroke symptoms. The stroke event needs to involve the middle cerebral artery (MCA) territory (cortical or subcortical) or posterior cerebral artery (PCA) territory with ischemic stroke confirmed by magnetic resonance imaging (MRI). Ischemic stroke is defined as death of an area of brain tissue (cerebral infarction) resulting from an inadequate supply of blood and oxygen to the brain.
- •National Institute of Health Stroke Scale (NIHSS) score ≥3 but <22 at the time of screening, at least 3 days after the onset of stroke symptoms. Patient should not have shown rapid improvement (≥8 point decrease since the onset of stroke symptoms) or deterioration (≥4 point increase since the beginning of screening) in the NIHSS score from time of initial evaluation to randomization. The time from initial evaluation to initial screening evaluation will be at least 72 hours.
- •New onset of extremity paresis on the affected side, defined as a score of 2 to 4 on the NIHSS Motor Arm (item 5) or Leg (item 6) question.
- •Must be alert or drowsy but easily arousable as defined by a score of 0 to 1 on the NIHSS Level of Consciousness question (item 1).
- •"Slow recovery" defined as change in NIHSS ≤1 point/3 days during the screening period.
- •Able to participate in the evaluation process to the point of accurate assessment with/without help.
- •Willing and able to comply with scheduled visits, lifestyle guidelines, treatment plan, laboratory tests, and other study procedures.
- •Must be willing to discontinue applying any topical preparations containing Vitamin A acids (including all-trans-retinoic acid [tretinoin], 13-cis-retinoic acid [isotretinoin], 9 cisretinoic acid [alitretinoin], vitamin A [retinol], retinal, and their derivatives) to any part of the body starting on Day 1 until study completion. (TF0023 may cause dry and/or itching skin. Curél Ultra Healing Lotion can be applied to the dry and/or itching skin).
排除标准
- •Pregnant or lactating female.
- •Any condition, including any significant medical or neuropsychiatric condition, including the presence of laboratory abnormalities, which in the judgment of the investigator places the patient at unacceptable risk if he/she were to participate in the study or confounds the ability to interpret data from the study including, but not limited to:
- •Aspartate transaminase (AST) or alanine transaminase (ALT) >3 × the upper limit of normal (ULN) at screening.
- •Serum creatinine concentration >1.5 times the ULN at screening. Estimated glomerular filtration rate (GFR) <60 mL/min/1.73 m2 is exclusionary.
- •Bilirubin or alkaline phosphatase level >2.5 × the ULN at screening.
- •Glucose <50 mg/dL or >450 mg/dL despite adequate anti-hyperglycemic treatment.
- •Platelet count <100 × 109/L.
- •History of bacteremia or other serious bacterial or fungal infection requiring treatment with intravenous antibiotics within 84 days (12 weeks) prior to treatment with study therapy other than a treated urinary tract infection.
- •Known infection with human immunodeficiency virus (HIV).
- •Seropositive for hepatitis C or hepatitis B.
- •Known history of seizures.
- •Evidence of cerebral hemorrhage within the last 6 months or recent intracerebral hematomas detected by brain CT or MRI.
- •Hypertension with systolic blood pressure (SBP) >185 mmHg or diastolic blood pressure (DBP) >120 mmHG (mean of 3 consecutive arm cuff readings over 20 to 30 minutes).
- •High clinical suspicion of septic embolus.
- •History of major trauma at time of stroke.
- •History of malignancy within 5 years except basal cell or squamous cell carcinoma of the skin or remote history of cancer now considered cured or positive Pap smear with subsequent negative follow up.
- •Known allergy to non-steroidal anti-inflammatory drugs (NSAIDs).
- •Known allergy to both gadolinium and iodine based contrast agents for MRI preventing the ability to conduct either one of these procedures.
- •Patient has received an investigational agent within 90 days or 5 half-lives, whichever is longer, prior to treatment with study therapy or planned participation in another therapeutic trial prior to the completion of this study.
- •Patients with very light neurological symptoms (NIHSS score of <3) or with rapidly improving symptoms before the start of treatment.
- •Patients with serious neurological disorders (NIHSS score ≥22) or serious consciousness disorders before the start of treatment.
- •Patients with functional disorders (mRS score >2) before onset of the stroke.
- •Patients who have been administered drugs that are not allowed to be administered concomitantly with any anti-thrombotic agents after onset of the stroke.
- •Patients who are forbidden to undergo DTI-MRI.
- •Patients with symptoms suggesting subarachnoid hemorrhage (SAH).
- •Patients with hemorrhage (gastrointestinal hemorrhage, urinary hemorrhage, retroperitoneal hemorrhage, or hemoptysis).
- •Patients who have been administered oral anticoagulants with values of the international normalized ratio (INR) of prothrombin time (PT-INR) >1.
- •Patients who have a history of intracranial hemorrhage, or who have a disease considered to increase the risk of intracranial hemorrhage such as an intracranial tumor, cerebral aneurysm, or intracranial arteriovenous malformation, etc.
- •Patients who were operated on or injured their head or spinal cord within 3 months before onset of the stroke.
- •Patients who have a history of gastrointestinal or urinary tract hemorrhage within 21 days before onset of the stroke.
- •Patients who had a major surgery or serious trauma (except for head or spinal cord trauma) within 14 days before onset of the stroke.
- •Patients who had an organ biopsy, arterial puncture, or lumbar puncture within 14 days before the onset of the stroke.
- •Patients with severe hepatic dysfunction or severe renal dysfunction.
- •Patients with acute pancreatitis.
- •Patients with concurrent infectious endocarditis, moyamoya disease (Willis circle occlusion syndrome), aortic dissection, or neck trauma, etc.
- •Patients judged to be difficult in monitoring for 4 to 7 months by their physician.
- •In addition to the above exclusion criteria, patients judged to be inadequate to participate in this study by their physician.
研究组 & 干预措施
High dose
75 patients will be randomized to active or placebo treatment in a 2:1 ratio (TF0023 [50 patients] and placebo [25 patients]). Each patient enrolled in Group A will receive study treatment in a double-blind manner for 16 weeks starting between 3 and 60 days after the onset of stroke symptoms (Day 1 of the study).
干预措施: TF0023 (Drug)
Middle dose
75 patients will be randomized to active or placebo treatment in a 2:1 ratio (TF0023 [50 patients] and placebo [25 patients]). Each patient enrolled in Group A will receive study treatment in a double-blind manner for 16 weeks starting between 3 and 60 days after the onset of stroke symptoms (Day 1 of the study).
干预措施: TF0023 (Drug)
Low dose
75 patients will be randomized to active or placebo treatment in a 2:1 ratio (TF0023 [50 patients] and placebo [25 patients]). Each patient enrolled in Group A will receive study treatment in a double-blind manner for 16 weeks starting between 3 and 60 days after the onset of stroke symptoms (Day 1 of the study).
干预措施: TF0023 (Drug)
结局指标
主要结局
The primary efficacy endpoint is the change from baseline in the mRS score for all randomized patients at Week 16 in Part A and Part B.
时间窗: 16 weeks of treatment
The mRS score measures the patient's functional level of activity and is dichotomized as a favorable outcome (score = 0 - 2) versus unfavorable (score ≥2). The mRS score ranges from 0 (no symptoms) to 6 (death) as follows: 0 = No symptoms at all 1. = No significant disability despite symptoms; able to carry out all usual duties and activities 2. = Slight disability; unable to carry out all previous activities, but able to look after own affairs without assistance 3. = Moderate disability requiring some help, but able to walk unassisted 4. = Moderate severe disability; unable to walk without assistance and unable to attend to own bodily needs without assistance. 5. = Severe disability; bedridden, incontinent, and requiring constant nursing care and attention. 6. = Dead.
次要结局
- Recurrent stroke after signing the informed consent form through Week 16 and Week 32.(16 and 32 weeks of treatment)
- NIHSS score changes after signing the informed consent form through Week 16 and Week 32.(0, 16 and 32 weeks of treatment)
- Volume of new fluid attenuation inversion recovery (FLAIR) lesions by DTI-MRI(16 and 32 weeks of treatment)
- Barthel Index (BI) changes after signing the informed consent form through Week 16 and Week 32.(0, 16 and 32 weeks of treatment)
- Death due to any cause after signing the informed consent form through Week 16 and Week 32.(16 and 32 weeks of treatment)
- Extended Glasgow Outcome Scale (GOS-E) changes after signing the informed consent form through Week 16 and Week 32.(0, 16 and 32 weeks of treatment)
- Shortening the time for performing the timed Trail-Making Tests(16 and 32 weeks of treatment)
- Blood flow in neck arteries by Ultrasonography after signing the informed consent form through Week 16 and Week 32.(16 and 32 weeks of treatment)
- Improvement of atherosclerosis in neck arteries by Ultrasonography after signing the informed consent form through Week 16 and Week 32.(16 and 32 weeks of treatment)
- Daily activities changes after signing the informed consent form through Week 16 and Week 32.(0, 16 and 32 weeks of treatment)
- Sleeping condition changes after signing the informed consent form through Week 16 and Week 32.(0, 16 and 32 weeks of treatment)
- Total cholesterol, triglycerides, high density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), and very low density lipoprotein cholesterol (VLDL C) changes(0, 16 and 32 weeks of treatment)
- Blood pressure changes after signing the informed consent form through Week 16 and Week 32.(0, 16 and 32 weeks of treatment)
- To access hemoglobin A1C (HbA1C) changes after signing the informed consent form through Week 16 and Week 32.(0, 16 and 32 weeks of treatment)
- To access patient's assessment of disease status(0, 16 and 32 weeks of treatment)
- To access investigator's assessment of disease status(0, 16 and 32 weeks of treatment)
- To access patient's assessment of response to therapy(16 and 32 weeks of treatment)
- To access investigator's assessment of response to therapy(16 and 32 weeks of treatment)