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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)

Studieoversigt

Status

Ikke rekrutterer endnu

Detaljeret beskrivelse

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.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

382

Fase

  • Fase 3

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

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

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

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.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Placebo komparator: Placebo
For oral administration. The placebo is identical to aprocitentan tablets(SYH9108) in appearance.
Eksperimentel: Aprocitentan tablets(SYH9108)
For oral administration

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change from baseline in Sitting Systolic Blood Pressure (SiSBP) after 8 weeks of treatment.
Tidsramme: 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

Sekundære resultatmål

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

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

31. maj 2026

Primær færdiggørelse (Anslået)

28. december 2029

Studieafslutning (Anslået)

31. maj 2030

Datoer for studieregistrering

Først indsendt

29. maj 2026

Først indsendt, der opfyldte QC-kriterier

3. juni 2026

Først opslået (Faktiske)

9. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

9. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

3. juni 2026

Sidst verificeret

1. juni 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • SYH9108-002

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med Resistent hypertension

Kliniske forsøg med Aprocitentan tablets(SYH9108)

Abonner