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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)

Studie Overzicht

Toestand

Nog niet aan het werven

Gedetailleerde beschrijving

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.

Studietype

Ingrijpend

Inschrijving (Geschat)

382

Fase

  • Fase 3

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

  • Naam: Clinical Trials Information Group officer
  • Telefoonnummer: +86311-69085587
  • E-mail: ctr-contact@cspc.cn

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

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.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Verviervoudigen

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Placebo-vergelijker: Placebo
For oral administration. The placebo is identical to aprocitentan tablets(SYH9108) in appearance.
Experimenteel: Aprocitentan tablets(SYH9108)
For oral administration

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change from baseline in Sitting Systolic Blood Pressure (SiSBP) after 8 weeks of treatment.
Tijdsspanne: 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

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change from baseline in SiSBP after 4 weeks of treatment
Tijdsspanne: 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.
Tijdsspanne: 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.
Tijdsspanne: 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.
Tijdsspanne: 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.
Tijdsspanne: 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.
Tijdsspanne: 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.
Tijdsspanne: 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.
Tijdsspanne: 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.
Tijdsspanne: 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.
Tijdsspanne: 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.
Tijdsspanne: 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.
Tijdsspanne: 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.
Tijdsspanne: 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.
Tijdsspanne: 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.
Tijdsspanne: 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).
Tijdsspanne: 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).
Tijdsspanne: Baseline up to approximately Week 10
AEs will be assessed using Mild/moderate/severe.
Baseline up to approximately Week 10

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

31 mei 2026

Primaire voltooiing (Geschat)

28 december 2029

Studie voltooiing (Geschat)

31 mei 2030

Studieregistratiedata

Eerst ingediend

29 mei 2026

Eerst ingediend dat voldeed aan de QC-criteria

3 juni 2026

Eerst geplaatst (Werkelijk)

9 juni 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

9 juni 2026

Laatste update ingediend die voldeed aan QC-criteria

3 juni 2026

Laatst geverifieerd

1 juni 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • SYH9108-002

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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