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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)

Aperçu de l'étude

Statut

Pas encore de recrutement

Les conditions

Description détaillée

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.

Type d'étude

Interventionnel

Inscription (Estimé)

382

Phase

  • Phase 3

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

  • Nom: Clinical Trials Information Group officer
  • Numéro de téléphone: +86311-69085587
  • E-mail: ctr-contact@cspc.cn

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

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.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Quadruple

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur placebo: Placebo
For oral administration. The placebo is identical to aprocitentan tablets(SYH9108) in appearance.
Expérimental: Aprocitentan tablets(SYH9108)
For oral administration

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change from baseline in Sitting Systolic Blood Pressure (SiSBP) after 8 weeks of treatment.
Délai: 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

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Change from baseline in SiSBP after 4 weeks of treatment
Délai: 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.
Délai: 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.
Délai: 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.
Délai: 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.
Délai: 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.
Délai: 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.
Délai: 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.
Délai: 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.
Délai: 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.
Délai: 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.
Délai: 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.
Délai: 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.
Délai: 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.
Délai: 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.
Délai: 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).
Délai: 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).
Délai: Baseline up to approximately Week 10
AEs will be assessed using Mild/moderate/severe.
Baseline up to approximately Week 10

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

31 mai 2026

Achèvement primaire (Estimé)

28 décembre 2029

Achèvement de l'étude (Estimé)

31 mai 2030

Dates d'inscription aux études

Première soumission

29 mai 2026

Première soumission répondant aux critères de contrôle qualité

3 juin 2026

Première publication (Réel)

9 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

9 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

3 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • SYH9108-002

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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