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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

Aprocitentan tablets are currently the only endothelin dual receptor antagonist approved internationally for the treatment of resistant hypertension.This is a multicenter, randomized, double-blind, placebo-controlled Phase 3 study to evaluate the efficacy and safety of aprocitentan tablets(SYH9108) in patients with treatment-resistant hypertension (rHTN)

연구 개요

상태

아직 모집하지 않음

상세 설명

The study consists of a screening period (up to 2 weeks), a run-in period (4 weeks), a treatment period (8 weeks), and a follow-up period. During the study, all participants should continue their background antihypertensive medications (at the same agents and dosages as used within 4 weeks prior to screening) and maintain lifestyle interventions such as a low-salt diet.

연구 유형

중재적

등록 (추정된)

382

단계

  • 3단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

  • 이름: Clinical Trials Information Group officer
  • 전화번호: +86311-69085587
  • 이메일: ctr-contact@cspc.cn

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

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아니

설명

Inclusion Criteria:

  1. Male or female participants must be ≥18 years of age.
  2. 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.
  3. 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.
  4. 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:

  1. Presence of secondary hypertension.
  2. 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.
  3. 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.
  4. Have had unstable cardiac disease occurring within the period from 6 months prior to signing the ICF up to randomization.
  5. Have received dialysis at any time prior to signing the ICF or prior to randomization.
  6. Type 1 diabetes.
  7. Compliance with any background antihypertensive drug or placebo is <80% or >120% during the run-in period.
  8. 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.
  9. 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.
  10. Participated in other clinical trials and received at least one dose of study treatment within 12 weeks prior to signing the ICF.
  11. 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.
  12. History of drug abuse or alcohol abuse within 5 years prior to signing the ICF.
  13. 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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 네 배로

무기와 개입

참가자 그룹 / 팔
개입 / 치료
위약 비교기: 위약
For oral administration. The placebo is identical to aprocitentan tablets(SYH9108) in appearance.
실험적: Aprocitentan tablets(SYH9108)
For oral administration

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Change from baseline in Sitting Systolic Blood Pressure (SiSBP) after 8 weeks of treatment.
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
Change from baseline in SiSBP after 4 weeks of treatment
기간: 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.
기간: 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.
기간: 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.
기간: 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.
기간: 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.
기간: 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.
기간: 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.
기간: 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.
기간: 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.
기간: 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.
기간: 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.
기간: 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.
기간: 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.
기간: 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.
기간: 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).
기간: 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).
기간: Baseline up to approximately Week 10
AEs will be assessed using Mild/moderate/severe.
Baseline up to approximately Week 10

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 5월 31일

기본 완료 (추정된)

2029년 12월 28일

연구 완료 (추정된)

2030년 5월 31일

연구 등록 날짜

최초 제출

2026년 5월 29일

QC 기준을 충족하는 최초 제출

2026년 6월 3일

처음 게시됨 (실제)

2026년 6월 9일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 6월 9일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 6월 3일

마지막으로 확인됨

2026년 6월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • SYH9108-002

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

약물 및 장치 정보, 연구 문서

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미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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