HJB647 Phase 1b Study in Japanese Healthy Participants With Elevated Blood Pressure and Patients With Hypertension
A Phase 1b, Randomized, Participant- and Investigator- Blinded, Placebo-controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of HJB647 Following Single Ascending Dose and Up-titration Multiple Dose Administration in Japanese Healthy Participants With Elevated Blood Pressure and Patients With Hypertension
研究概览
详细说明
Randomized, placebo-controlled, participant- and investigator-blind study consisting of two parts:
- Part 1 (SAD part): Single oral dose in healthy participants. Sentinel dosing will be applied in each cohort.
- Part 2 (MAD part): Multiple oral doses in patients with hypertension. Safety reviews will guide dose escalation and up-titration.
研究类型
注册 (估计的)
阶段
- 阶段1
联系人和位置
学习联系方式
- 姓名:Novartis Pharmaceuticals
研究联系人备份
- 姓名:Novartis Pharmaceuticals
- 电话号码:+81337978748
- 邮箱:novartis.email@novartis.com
学习地点
-
-
Tokyo
-
Sumida Ku、Tokyo、日本、1300004
- 招聘中
- Novartis Investigative Site
-
-
参与标准
资格标准
适合学习的年龄
- 成人
接受健康志愿者
描述
Inclusion Criteria:
- Japanese healthy participants with elevated blood pressure (Part 1) and patients with mild-to-moderate hypertension (Part 2)
- Age: 18 to 55 years (Part 1) and 18 to 60 years (Part 2)
Body weight:
- Male: ≥ 50.0 kg
- Female: ≥ 45.0 kg
- Body Mass Index (BMI): 18.0 to 30.0 kg/m²
- Axillary body temperature: 35.0-37.5 °C
- Heart rate: 50-90 bpm
Blood pressure criteria are as follows:
- Part 1: Healthy Participants with Elevated Blood Pressure Screening: Systolic Blood Pressure (SBP): 120 ≤ SBP ≤ 139 mmHg; Diastolic Blood Pressure (DBP): 60 ≤ DBP ≤ 94 mmHg Baseline (Day -1): SBP: 120 ≤ SBP ≤ 179 mmHg; DBP: 60 ≤ DBP ≤ 109 mmHg
- Part 2: Patients with Hypertension Screening and Baseline (Day -1): SBP: 140 ≤ SBP ≤ 179 mmHg; DBP: 60 ≤ DBP ≤ 109 mmHg
Exclusion Criteria:
- Significant illness, including infectious diseases that have not resolved within 30 days prior to baseline
History or current diagnosis of ECG or cardiac abnormalities indicating significant risk of safety for participants such as:
- Concomitant clinically significant cardiac arrhythmias, e.g., sustained ventricular tachycardia, and clinically significant second- or third-degree AV block without a pacemaker.
- History of familial long QT syndrome or known family history of Torsades de Pointes
- Resting QT interval corrected by Fridericia's formula (QTcF) ≥ 450 msec (male) or ≥ 460 msec (female) at screening
- At screening, hypokalemia or hypomagnesemia defined as potassium or magnesium values below the LLN on repeat measurement, or laboratory abnormalities indicating hypothyroidism, as determined at the discretion of the investigator
- HbA1c ≥ 7.0% or LDL cholesterol ≥ 180 mg/dL or triglycerides ≥ 250 mg/dL
- Use of any prescription drugs or herbal supplements within 4 weeks prior to initial dosing, and/or OTC medication or dietary supplements (vitamins included) within 2 weeks prior to initial dosing
- Women of childbearing potential
Other protocol-defined inclusion/exclusion criteria may apply
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Part 1-1: HJB647 low dose
Single dose Day 1 in Part 1
|
HJB647 oral capsule
|
|
实验性的:Part 1-2: HJB647 mid-dose
Single dose Day 1 in Part 1
|
HJB647 oral capsule
|
|
实验性的:Part 1-3: HJB647 high dose
Single dose Day 1 in Part 1
|
HJB647 oral capsule
|
|
安慰剂比较:Part 1: Placebo
Single dose Day 1 in Part 1
|
匹配的口服安慰剂
|
|
实验性的:Part 2-1: HJB647 multiple oral doses
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
|
HJB647 oral capsule
|
|
实验性的:Part 2-2: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
|
HJB647 oral capsule
|
|
实验性的:Part 2-3: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
|
HJB647 oral capsule
|
|
实验性的:Part 2-4: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
|
HJB647 oral capsule
|
|
实验性的:Part 2-5: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
|
HJB647 oral capsule
|
|
安慰剂比较:Part 2: Placebo
Multiple oral doses of placebo with adaptive up-titration in Part 2
|
匹配的口服安慰剂
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Part 1: Cmax
大体时间:Part 1 on Day 1
|
Cmax: The maximum (peak) observed plasma, blood, serum, or other body fluid drug concentration after single dose administration (mass x volume-1)
|
Part 1 on Day 1
|
|
Part 1: Tmax
大体时间:Part 1 on Day 1
|
Tmax: The time to reach maximum (peak) plasma, blood, serum, or other body fluid drug concentration after single dose administration (time)
|
Part 1 on Day 1
|
|
Part 1: AUClast
大体时间:Part 1 on Day 1
|
AUClast: The AUC from time zero to the last measurable concentration sampling time (tlast) (mass x time x volume-1)
|
Part 1 on Day 1
|
|
Part 1: AUCinf
大体时间:Part 1 on Day 1
|
AUCinf: The AUC from time zero to infinity (mass x time x volume-1)
|
Part 1 on Day 1
|
|
Part 1: T1/2
大体时间:Part 1 on Day 1
|
T1/2: The elimination half-life associated with the terminal slope (λz) of a semi logarithmic concentration-time curve (time).
Use qualifier for other half-lives
|
Part 1 on Day 1
|
|
Part 2: Number of participants with AEs
大体时间:Up to 51 days
|
Number of participants with adverse events (AEs) including abnormal vital signs, ECG, and safety laboratory parameters
|
Up to 51 days
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Part 2: Cmax
大体时间:Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
|
Cmax: The maximum (peak) observed plasma, blood, serum, or other body fluid drug concentration after single dose administration (mass x volume-1)
|
Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
|
|
Part 2: Tmax
大体时间:Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
|
Tmax: The time to reach maximum (peak) plasma, blood, serum, or other body fluid drug concentration after single dose administration (time)
|
Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
|
|
Part 2: AUClast
大体时间:Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
|
AUClast: The AUC from time zero to the last measurable concentration sampling time (tlast) (mass x time x volume-1)
|
Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
|
|
Part 2: AUCinf
大体时间:Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
|
AUCinf: The AUC from time zero to infinity (mass x time x volume-1)
|
Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
|
|
Part 2: AUCtau
大体时间:Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
|
AUCtau: The AUC calculated to the end of a dosing interval (tau) at steady-state (amount x time x volume-1)
|
Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
|
|
Part 2: T1/2
大体时间:Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
|
T1/2: The elimination half-life associated with the terminal slope (λz) of a semi logarithmic concentration-time curve (time).
Use qualifier for other half-lives
|
Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
|
|
Part 1: Number of participants with AEs
大体时间:Up to 31 days
|
Number of participants with adverse events (AEs) including abnormal vital signs, ECG, and safety laboratory parameters
|
Up to 31 days
|
|
Part 2: Office blood pressure change from baseline
大体时间:Baseline to Day 27 of part 2
|
Change in office blood pressure from baseline
|
Baseline to Day 27 of part 2
|
|
Part 2: Heart rate change from baseline
大体时间:Baseline to Day 27 of part 2
|
Change in heart rate from baseline
|
Baseline to Day 27 of part 2
|
合作者和调查者
调查人员
- 研究主任:Novartis Pharmaceuticals、Novartis Pharmaceuticals
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
关键字
其他研究编号
- CHJB647A11101
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
Novartis is committed to sharing with qualified external researchers, access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations.
This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.