- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT07635914
A Study Evaluating Aprocitentan Tablets(SYH9108) for the Treatment of Resistant Hypertension
A Multicenter, Randomized, Double-blind, Placebo-controlled Phase 3 Study of Aprocitentan Tablets in the Treatment of Resistant Hypertension
Обзор исследования
Статус
Условия
Вмешательство/лечение
Подробное описание
Тип исследования
Регистрация (Оцененный)
Фаза
- Фаза 3
Контакты и местонахождение
Контакты исследования
- Имя: Clinical Trials Information Group officer
- Номер телефона: +86311-69085587
- Электронная почта: ctr-contact@cspc.cn
Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
- Взрослый
- Пожилой взрослый
Принимает здоровых добровольцев
Описание
Inclusion Criteria:
- Male or female participants must be ≥18 years of age.
- Participants must have received stable doses of ≥3 antihypertensive agents from distinct pharmacological classes for at least 4 weeks prior to signing the ICF, with such therapy maintained until randomization.
- During the screening period and prior to randomization, SiSBP ≥140 mmHg with or without SiDBP ≥90 mmHg, and SiSBP <180 mmHg and SiDBP <110 mmHg.
- Participants are able to understand and cooperate in completing this trial, voluntarily participate in the trial, and sign the Informed Consent Form (ICF).
Exclusion Criteria:
- Presence of secondary hypertension.
- Have had transient ischemic attack, stroke, unstable angina pectoris, or acute myocardial infarction occurring within the period from 12 months prior to signing the ICF up to randomization.
- From screening to prior to randomization, have presence of uncontrolled severe disease or life-threatening disease, or failure to recover from major surgery, or prior thyroid surgery, or presence of malignant tumor, or meeting the criteria for severe hepatic insufficiency at screening.
- Have had unstable cardiac disease occurring within the period from 6 months prior to signing the ICF up to randomization.
- Have received dialysis at any time prior to signing the ICF or prior to randomization.
- Type 1 diabetes.
- Compliance with any background antihypertensive drug or placebo is <80% or >120% during the run-in period.
- Use of endothelin receptor antagonists, antihypertensive drugs other than background medications, or other blood pressure-affecting drugs, or high-dose loop diuretics from 4 weeks prior to signing the ICF until randomization; or use of oligonucleotide antihypertensive agents within 1 year prior to signing the ICF.
- Hypersensitivity or suspected hypersensitivity to the excipients of the investigational product, endothelin receptor antagonists, or background antihypertensive drugs, or potential hypersensitivity to the investigational product.
- Participated in other clinical trials and received at least one dose of study treatment within 12 weeks prior to signing the ICF.
- Average night shifts are ≥ 2 times per week during the 4 weeks prior to signing the ICF, the screening period, the run-in period, or the anticipated study period.
- History of drug abuse or alcohol abuse within 5 years prior to signing the ICF.
- Any of the following test results during the screening period or prior to randomization:
1) BMI≥37.5 kg/m2. 2) Hemoglobin < 100 g/L; 3) NT-proBNP ≥ 500 pg/mL; 4) QTcF: > 450 ms in males, > 470 ms in females; 5) eGFR < 15 mL/min/1.73 m²; 6) ALT or AST > 3 × ULN, or total bilirubin > 1.5 × ULN; 7) HbA1c > 8.0%; 8) TSH outside the normal range and FT3 and/or FT4 outside the normal range; 9) Positive HBsAg and positive HBV-DNA, or positive for any of anti-HCV antibody, anti-HIV antibody, anti-Treponema pallidum antibody.
14. Female participants of childbearing potential who are pregnant, breastfeeding, or have a positive pregnancy test from signing the ICF until randomization; or female participants of childbearing potential and male participants who plan to conceive (including sperm or egg donation) and/or are unable to use effective contraceptive methods during the study period and within 30 days after the end of treatment.
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Рандомизированный
- Интервенционная модель: Параллельное назначение
- Маскировка: Четырехместный
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
|
Плацебо Компаратор: Плацебо
|
For oral administration.
The placebo is identical to aprocitentan tablets(SYH9108) in appearance.
|
|
Экспериментальный: Aprocitentan tablets(SYH9108)
|
For oral administration
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Change from baseline in Sitting Systolic Blood Pressure (SiSBP) after 8 weeks of treatment.
Временное ограничение: Baseline and week 8
|
To assess the effect of treatment with Aprocitentan tablets(SYH9108) versus placebo on SiSBP at Week 8.
|
Baseline and week 8
|
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Change from baseline in SiSBP after 4 weeks of treatment
Временное ограничение: Baseline and week 4
|
To assess the effect of treatment with Aprocitentan tablets(SYH9108) versus placebo.
|
Baseline and week 4
|
|
Change from baseline in Sitting Diastolic Blood Pressure (SiSDP) after 4 weeks of treatment.
Временное ограничение: Baseline and week 4
|
To assess the effect of treatment with Aprocitentan tablets(SYH9108) versus placebo.
|
Baseline and week 4
|
|
Change from baseline in SiSDP after 8 weeks of treatment.
Временное ограничение: Baseline and week 8
|
To assess the effect of treatment with Aprocitentan tablets(SYH9108) versus placebo.
|
Baseline and week 8
|
|
Change from baseline in ambulatory 24-hour average SBP after 4 weeks of treatment.
Временное ограничение: Baseline and week 4
|
To assess the effect of treatment with Aprocitentan tablets(SYH9108) versus placebo.
|
Baseline and week 4
|
|
Change from baseline in ambulatory 24-hour average SDP after 4 weeks of treatment.
Временное ограничение: Baseline and week 4
|
To assess the effect of treatment with Aprocitentan tablets(SYH9108) versus placebo.
|
Baseline and week 4
|
|
Change from baseline in ambulatory 24-hour average SBP after 8 weeks of treatment.
Временное ограничение: Baseline and week 8
|
To assess the effect of treatment with Aprocitentan tablets(SYH9108) versus placebo
|
Baseline and week 8
|
|
Change from baseline in ambulatory 24-hour average SDP after 8 weeks of treatment.
Временное ограничение: Baseline and week 8
|
To assess the effect of treatment with Aprocitentan tablets(SYH9108) versus placebo
|
Baseline and week 8
|
|
Change from baseline in ambulatory night-time average SBP after 4 weeks of treatment.
Временное ограничение: Baseline and week 4
|
To assess the effect of treatment with Aprocitentan tablets(SYH9108) versus placebo.
|
Baseline and week 4
|
|
Change from baseline in ambulatory night-time average SDP after 4 weeks of treatment.
Временное ограничение: Baseline and week 4
|
To assess the effect of treatment with Aprocitentan tablets(SYH9108) versus placebo.
|
Baseline and week 4
|
|
Change from baseline in ambulatory night-time average SBP after 8 weeks of treatment.
Временное ограничение: Baseline and week 8
|
To assess the effect of treatment with Aprocitentan tablets(SYH9108) versus placebo.
|
Baseline and week 8
|
|
Change from baseline in ambulatory night-time average SDP after 8 weeks of treatment.
Временное ограничение: Baseline and week 8
|
To assess the effect of treatment with Aprocitentan tablets(SYH9108) versus placebo.
|
Baseline and week 8
|
|
Change from baseline in ambulatory daytime average SBP after 4 weeks of treatment.
Временное ограничение: Baseline and week 4
|
To assess the effect of treatment with Aprocitentan tablets(SYH9108) versus placebo.
|
Baseline and week 4
|
|
Change from baseline in ambulatory daytime average SDP after 4 weeks of treatment.
Временное ограничение: Baseline and week 4
|
To assess the effect of treatment with Aprocitentan tablets(SYH9108) versus placebo.
|
Baseline and week 4
|
|
Change from baseline in ambulatory daytime average SBP after 8 weeks of treatment.
Временное ограничение: Baseline and week 8
|
To assess the effect of treatment with Aprocitentan tablets(SYH9108) versus placebo.
|
Baseline and week 8
|
|
Change from baseline in ambulatory daytime average SDP after 8 weeks of treatment.
Временное ограничение: Baseline and week 8
|
To assess the effect of treatment with Aprocitentan tablets(SYH9108) versus placebo.
|
Baseline and week 8
|
|
Number of Participants with Treatment Emergent Adverse Events (TEAEs).
Временное ограничение: Baseline up to approximately Week 10
|
AEs will be assessed using Mild/moderate/severe.
|
Baseline up to approximately Week 10
|
|
Number of Participants with Serious Adverse Events (SAEs).
Временное ограничение: Baseline up to approximately Week 10
|
AEs will be assessed using Mild/moderate/severe.
|
Baseline up to approximately Week 10
|
Соавторы и исследователи
Даты записи исследования
Изучение основных дат
Начало исследования (Оцененный)
Первичное завершение (Оцененный)
Завершение исследования (Оцененный)
Даты регистрации исследования
Первый отправленный
Впервые представлено, что соответствует критериям контроля качества
Первый опубликованный (Действительный)
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
Последнее отправленное обновление, отвечающее критериям контроля качества
Последняя проверка
Дополнительная информация
Термины, связанные с этим исследованием
Ключевые слова
Другие идентификационные номера исследования
- SYH9108-002
Планирование данных отдельных участников (IPD)
Планируете делиться данными об отдельных участниках (IPD)?
Информация о лекарствах и устройствах, исследовательские документы
Изучает лекарственный продукт, регулируемый FDA США.
Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.
Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .