- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07635914
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
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
Studietype
Registrering (Antatt)
Fase
- Fase 3
Kontakter og plasseringer
Studiekontakt
- Navn: Clinical Trials Information Group officer
- Telefonnummer: +86311-69085587
- E-post: ctr-contact@cspc.cn
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Beskrivelse
Inclusion Criteria:
- Male or female participants must be ≥18 years of age.
- 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.
- 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.
- 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:
- Presence of secondary hypertension.
- 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.
- 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.
- Have had unstable cardiac disease occurring within the period from 6 months prior to signing the ICF up to randomization.
- Have received dialysis at any time prior to signing the ICF or prior to randomization.
- Type 1 diabetes.
- Compliance with any background antihypertensive drug or placebo is <80% or >120% during the run-in period.
- 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.
- 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.
- Participated in other clinical trials and received at least one dose of study treatment within 12 weeks prior to signing the ICF.
- 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.
- History of drug abuse or alcohol abuse within 5 years prior to signing the ICF.
- 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
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
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Andre studie-ID-numre
- SYH9108-002
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
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