A Randomized, Double-blind, Placebo-controlled, Multiple Dose Study to Evaluate the Safety and Tolerability of a Once Daily Dose of 50 mg E2609 in Healthy Japanese Subjects
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 16
- 试验地点
- 1
- 主要终点
- Number of participants with any serious adverse event and number of participants with any non-serious adverse event
研究概览
简要总结
Study E2609-J081-014 is a single-center, randomized, double-blind, placebo-controlled study conducted to evaluate the safety and tolerability of multiple oral doses of E2609 50 milligrams (mg), administered once daily for 14 days, in healthy Japanese participants aged 50 to 85 years.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Basic Science
- 盲法
- Triple (Participant, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 50 Years 至 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Healthy males and females
- •Aged 50 to 85 years, inclusive at time of consent
- •Body mass index (BMI) of 17.6 to 32 kilograms per meters squared (kg/m^2) at Screening
排除标准
- •Personal or family history of seizure disorder, symptomatic seizures (not including a history of simple febrile seizures in childhood) or any past or present medical condition which, in the opinion of the investigator has the potential to reduce seizure threshold (eg, history of head trauma or concussion, previous alcohol abuse, substance abuse)
- •A history of cerebrovascular accident or non-vasovagal-related loss of consciousness
- •Any clinically significant findings on neurological examination
- •A family history of Long QT Syndrome or a presence of other risk factors for Torsades de Pointes (TDP), such as hypokalemia, hypomagnesemia, or hypocalcemia
- •History of cardiac arrhythmias, ischemic heart disease, or cerebrovascular disease
- •A history of gastrointestinal surgery that may affect the pharmacokinetic profile of E2609 (eg, hepatectomy, nephrotomy, digestive organ resection)
- •A known history of clinically significant drug or food allergies or presently experiencing significant seasonal allergy
研究组 & 干预措施
E2609 50 mg
Participants will receive E2609 50 milligrams (mg) orally once a day for 14 days.
干预措施: E2609 (Drug)
Placebo
Participants will receive matching placebo orally once a day for 14 days.
干预措施: Placebo (Drug)
结局指标
主要结局
Number of participants with any serious adverse event and number of participants with any non-serious adverse event
时间窗: up to Day 35 (Termination/Visit 5)
An adverse event is defined as any untoward medical occurrence associated with the use of a drug in humans, whether or not considered drug related. A serious adverse event is defined as any adverse event occurring at any dose that results in any of the following outcomes: results in death; is life threatening; results in inpatient hospitalization or prolongation of existing hospitalization; results in a persistent or significant incapacity or substantial disruption of the ability to conduct normal life function; results in a congenital anomaly/birth defect; or can be defined as any other important medical event.
Number of participants with an abnormal, clinically significant laboratory test value
时间窗: Screening; Baseline; Days 4, 8, 11, 14, 20 (Out-Patient Follow-up), and 35 (Termination/Visit 5); up to Day 62 (unscheduled Follow-up visits)
Laboratory test values will be assigned a low/normal/high (LNH) classification according to whether the value was below (L), within (N), or above (H) the laboratory parameter's reference range. Clinical significance will be determined by the Investigator.
Number of participants with an abnormal, clinically significant vital sign value
时间窗: Screening; Baseline; up to Day 62
Vital sign measurements (ie, systolic and diastolic blood pressure \[BP\] \[millimeters of mercury (mmHg)\], heart rate \[beats per minute\], respiratory rate \[breaths per minute\], body temperature \[centigrade\]) will be obtained in the supine position by a validated method. Clinical significance will be determined by the Investigator.
Number of participants with an abnormal, clinically significant electrocardiogram (ECG) finding
时间窗: Screening; Baseline; up to Day 62
Twelve-lead standard ECGs will be recorded in triplicate. ECGs will be recorded after the participant has been in the supine position for at least 10 minutes before and during the reading. In addition, all ECGs will be obtained before blood draws. Clinical significance will be determined by the Investigator.
Clinical assessment of suicidality per the suicidality rating scale
时间窗: Baseline (Day -1), 24 hours after dosing (Day 2), Day 15, Day 20, Day 35 (Termination/Visit 5), up to Day 62 (unscheduled Follow-up visits)
The suicidality rating scale will rate a participant's degree of suicidal ideation on a scale, ranging from "wish to be dead" to "active suicidal ideation with specific plan and intent." The decision to classify an isolated suicidality rating scale response as an adverse event will be exercised through medical and scientific judgment.
Mean quality of sleep score per the Waketime Questionnaire, if necessary
时间窗: up to Day 62
Participants reporting adverse events (AEs) relating to abnormal dreams, nightmares, or sleep terrors will be questioned using the Waketime Questionnaire which is comprised of 5 individual questions. A participant is asked to rate the quality of their sleep as: 1, Very sound or restful; 2, Sound or restful; 3, Average quality; 4, Restless; or 5, Very restless.
次要结局
- Number of participants with polymorphisms of N-acetyltransferase 2 (NAT2)(Day 1)
- Median time from dosing to reach Cmax (tmax) of E2609 and metabolites on Day 1 and Day 14(Days 1 and 14: predose; 1, 2, 3, 4, 6, and 10 hours postdose)
- Mean area under the concentration-time curve (AUC) from time 0 to 24 hours for E2609 and metabolites on Day 1 and Day 14(Days 1 and 14: 1, 2, 3, 4, 6, 10, and 24 hours postdose)
- Mean terminal elimination half-life (t1/2) following the last day of dosing (Day 14) of E2609 and metabolites(Day 14: 1, 2, 3, 4, 6, 10, 24, 48, 72, 96, and 144 hours postdose)
- Mean average concentration calculated as AUCss/tau (Css,av), where tau is the dosing interval, of E2609 and metabolites on Day 1 and Day 14(Days 1 and 14: 1, 2, 3, 4, 6, 10, and 24 hours postdose)
- Mean accumulation ratio for AUC, Cmax, and Cmin (Rac) for E2609 and metabolites on Day 1 and Day 14(Days 1 and 14: 1, 2, 3, 4, 6, 10, and 24 hours postdose)
- Mean maximum observed concentration (Cmax) of E2609 and metabolites on Day 1 and Day 14(Days 1 and 14: predose; 1, 2, 3, 4, 6, and 10 hours postdose)
- Mean minimum observed concentration (Cmin) of E2609 and metabolites on Day 1 and Day 14(Days 1 and 14: predose; 1, 2, 3, 4, 6, and 10 hours postdose)
- Apparent clearance at steady state (CLss/F) of E2609 on Day 14(Day 14: 1, 2, 3, 4, 6, 10, 24, 48, 72, 96, and 144 hours postdose)