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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)

Studieoversikt

Status

Har ikke rekruttert ennå

Detaljert 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.

Studietype

Intervensjonell

Registrering (Antatt)

382

Fase

  • Fase 3

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

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

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

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

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Firemannsrom

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Placebo komparator: Placebo
For oral administration. The placebo is identical to aprocitentan tablets(SYH9108) in appearance.
Eksperimentell: Aprocitentan tablets(SYH9108)
For oral administration

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
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
Tiltaksbeskrivelse
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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

31. mai 2026

Primær fullføring (Antatt)

28. desember 2029

Studiet fullført (Antatt)

31. mai 2030

Datoer for studieregistrering

Først innsendt

29. mai 2026

Først innsendt som oppfylte QC-kriteriene

3. juni 2026

Først lagt ut (Faktiske)

9. juni 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

9. juni 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

3. juni 2026

Sist bekreftet

1. juni 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • SYH9108-002

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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