A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Safety, Tolerability and Pharmacokinetic Study of Escalating Multiple Doses of TAK-935 in Healthy Subjects
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Percentage of Participants Who Experience at Least One Treatment-emergent Adverse Event (TEAE)
研究概览
简要总结
The purpose of this study is to assess the safety, tolerability and pharmacokinetics (PK) of multiple rising doses of TAK-935 in healthy participants.
详细描述
The drug being tested in this study is called TAK-935. This study will look at the pharmacokinetics, safety and tolerability of TAK-935 in healthy participants. The study will enroll approximately 56 participants. Participants will be randomly assigned (by chance, like flipping a coin) to 1 of the 5 cohorts in Part 1, which will remain undisclosed to the participant and study doctor during the study (unless there is an urgent medical need):
- Part 1, Cohort 1: TAK-935 100 mg QD
- Part 1, Cohort 2: TAK-935 300 mg QD
- Part 1, Cohort 3: TAK-935 300 mg BID
- Part 1, Cohort 4: TAK-935 600 mg QD
- Part 1, Cohort 5: TAK-935 400 mg QD Participants will be asked to take the oral solution once or twice a day at the same time for 14 days. An optional Part 2 may be conducted for collecting data to assess the engagement by TAK-935 of the central molecular target cholesterol 24S-hydroxylase (CH24H) by measuring the changes of levels of the metabolite 24S-hydroxycholesterol (24HC). In Part 2, participants will be assigned to up to 2 treatment groups at doses based on the data from other ongoing TAK-935 trials, combined with the safety and tolerability data from Cohorts 1-4 of Part 1.
This single center trial will be conducted in the United States. The overall time to participate in this study will be approximately 30 days. Participants will be admitted in the clinic for the first 14 days, and will be contacted by telephone on Day 28 for a follow-up assessment.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 55 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •All Cohorts
- •Is capable of understanding and complying with protocol requirements.
- •Signs and dates a written, informed consent form and any required privacy authorization prior to the initiation of any study procedures including requesting that a participant fast for any laboratory evaluations.
- •Is a healthy male or female aged 18 to 55 years inclusive, at the time of informed consent and first study medication dose.
- •Weighs at least 45 kilogram (kg) and has a body mass index (BMI) from 18.0 to 30.0 kilogram per square meter (kg/m^2), inclusive at Screening and Day -
- •Male participant who is non-sterilized and sexually active with a female partner of childbearing potential agrees to use adequate contraception from signing of informed consent throughout the duration of the study and for 30 days after last dose.
- •Female participant of childbearing potential who is sexually active with a non-sterilized male partner agrees to use routinely adequate contraception from signing of informed consent and throughout the duration of the study, and for 30 days after the last dose.
- •Can complete the CogState Battery at Screening.
- •Additional Inclusion Criteria for Participants undergoing cerebrospinal fluid (CSF) Sampling (Part 2 only):
- •Agrees to spinal tap procedures for CSF collection.
排除标准
- •All Cohorts
- •Has received any investigational compound within 30 days prior to randomization.
- •Has received TAK-935 in a previous clinical study or as a therapeutic agent.
- •Has a significant history of uncontrolled, clinically significant neurologic (including seizure disorders), cardiovascular, pulmonary, hepatic, renal, metabolic, gastrointestinal, urologic, immunologic, endocrine disease or psychiatric disorder or endocrine disease or other abnormality or any significant results from physical examinations, or clinical laboratory results which may impact the ability of the participant to participate or potentially confound the study results. It is the responsibility of the investigator to assess the clinical significance; however, consultation with the Takeda Medical Monitor may be warranted.
- •Has a known hypersensitivity to any component of the formulation of TAK-
- •Has a history of drug abuse (defined as any illicit drug use) or a history of alcohol abuse within 1 year prior to the screening visit or is unwilling to agree to abstain from alcohol and drugs throughout the study. One unit is equivalent to a half-pint of beer or a single measure of spirits or 1 small glass of wine.
- •Has taken any excluded medication, supplements, or food products during the time periods listed in the Excluded Medications and Dietary Products table.
- •Additional Exclusion Criteria for Participants undergoing CSF sampling (Part 2)
- •Has CSF collection performed within 30 days prior to check-in (Day -3).
- •Has a known hypersensitivity to the anesthetic or its derivatives used during CSF collection, or any medication used to prepare the area of lumbar puncture.
- •Has significant vertebral deformities (scoliosis or kyphosis) which, in the opinion of the investigator, may interfere with lumbar puncture procedure.
- •Has a history of clinically significant back pain and/or injury.
- •Has local infection at the puncture site.
研究组 & 干预措施
Part 1, Cohort 1: TAK-935 100 mg QD
TAK-935 100 milligram (mg), solution, orally, once daily (QD) or TAK-935 placebo-matching solution, orally, QD for up to 14 days.
干预措施: TAK-935 (Drug)
Part 1, Cohort 2: TAK-935 300 mg QD
TAK-935 300 mg, solution, orally, QD or TAK-935 placebo-matching solution, orally, QD for up to 14 days.
干预措施: TAK-935 (Drug)
Part 1, Cohort 4: TAK-935 600 mg QD
TAK-935 600 mg, solution, orally, QD or TAK-935 placebo-matching solution, orally, QD for up to 10 days.
干预措施: TAK-935 (Drug)
Part 2, Cohort 7: TAK-935 Dose 2
TAK-935 second decided dose as determined from other TAK-935 trials and Cohorts 1 to 4 of Part 1, solution, orally, QD or TAK-935 placebo-matching solution, orally, QD for up to 14 days.
干预措施: Placebo (Drug)
Part 1, Cohort 5: TAK-935 400 mg QD
TAK-935 400 mg, solution, orally, QD or TAK-935 placebo-matching solution, orally, QD for up to 14 days.
干预措施: Placebo (Drug)
Part 2, Cohort 6: TAK-935 Dose 1
TAK-935 first decided dose as determined from other TAK-935 trials and Cohorts 1 to 4 of Part 1, solution, orally, QD or TAK-935 placebo-matching solution, orally, QD for up to 14 days.
干预措施: TAK-935 (Drug)
Part 2, Cohort 6: TAK-935 Dose 1
TAK-935 first decided dose as determined from other TAK-935 trials and Cohorts 1 to 4 of Part 1, solution, orally, QD or TAK-935 placebo-matching solution, orally, QD for up to 14 days.
干预措施: Placebo (Drug)
Part 2, Cohort 7: TAK-935 Dose 2
TAK-935 second decided dose as determined from other TAK-935 trials and Cohorts 1 to 4 of Part 1, solution, orally, QD or TAK-935 placebo-matching solution, orally, QD for up to 14 days.
干预措施: TAK-935 (Drug)
Part 1, Cohort 3: TAK-935 300 mg BID
TAK-935 300 mg, solution, orally, twice daily (BID) or TAK-935 placebo-matching solution, orally, BID for up to 10 days.
干预措施: Placebo (Drug)
Part 1, Cohort 4: TAK-935 600 mg QD
TAK-935 600 mg, solution, orally, QD or TAK-935 placebo-matching solution, orally, QD for up to 10 days.
干预措施: Placebo (Drug)
Part 1, Cohort 5: TAK-935 400 mg QD
TAK-935 400 mg, solution, orally, QD or TAK-935 placebo-matching solution, orally, QD for up to 14 days.
干预措施: TAK-935 (Drug)
Part 1, Cohort 1: TAK-935 100 mg QD
TAK-935 100 milligram (mg), solution, orally, once daily (QD) or TAK-935 placebo-matching solution, orally, QD for up to 14 days.
干预措施: Placebo (Drug)
Part 1, Cohort 2: TAK-935 300 mg QD
TAK-935 300 mg, solution, orally, QD or TAK-935 placebo-matching solution, orally, QD for up to 14 days.
干预措施: Placebo (Drug)
Part 1, Cohort 3: TAK-935 300 mg BID
TAK-935 300 mg, solution, orally, twice daily (BID) or TAK-935 placebo-matching solution, orally, BID for up to 10 days.
干预措施: TAK-935 (Drug)
结局指标
主要结局
Percentage of Participants Who Experience at Least One Treatment-emergent Adverse Event (TEAE)
时间窗: Day 1 up to Day 28
Percentage of Participants Who Meet the Takeda Markedly Abnormal Criteria for Safety Laboratory Tests at Least Once Post Dose
时间窗: Baseline up to Day 15
Percentage of Participants Who Meet the Takeda Markedly Abnormal Criteria for Vital Sign Measurements at Least Once Post Dose
时间窗: Baseline up to Day 15
Percentage of Participants Who Meet the Takeda Markedly Abnormal Criteria for Safety 12-lead Electrocardiogram (ECG) Parameters at Least Once Post Dose
时间窗: Baseline up to Day 15
次要结局
- Cmax: Maximum Observed Plasma Concentration for TAK-935(Day 1 and Day 14: Pre-dose and at multiple time points (up to 24 hours for Cohorts 1, 2, 4, and 5; up to 12 hours for Cohort 3) post-dose)
- AUClast: Area Under the Plasma Concentration-time Curve From Time 0 to the Time of the Last Quantifiable Concentration for TAK-935(Day 1 and Day 14: Pre-dose and at multiple time points (up to 24 hours for Cohorts 1, 2, 4, and 5; up to 12 hours for Cohort 3) post-dose)
- AUC∞: Area Under the Plasma Concentration-time Curve From Time 0 to Infinity for TAK-935(Day 1: Pre-dose and at multiple time points (up to 24 hours for Cohorts 1, 2, 4, and 5; up to 12 hours for Cohort 3) post-dose)
- AUCτ: Area Under the Plasma Concentration-time Curve From Time 0 to Over the Dosing Interval for TAK-935(Day 14: Pre-dose and at multiple time points (up to 24 hours for Cohorts 1, 2, 4, and 5; up to 12 hours for Cohort 3) post-dose)