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HJB647 Phase 1b Study in Japanese Healthy Participants With Elevated Blood Pressure and Patients With Hypertension

21. juli 2026 oppdatert av: Novartis Pharmaceuticals

A Phase 1b, Randomized, Participant- and Investigator- Blinded, Placebo-controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of HJB647 Following Single Ascending Dose and Up-titration Multiple Dose Administration in Japanese Healthy Participants With Elevated Blood Pressure and Patients With Hypertension

The purpose of this study is to assess the safety, tolerability, pharmacokinetics and pharmacokinetics, and pharmacodynamics of HJB647 following single dose administration in Japanese healthy participants with elevated blood pressure and multiple dose administration with up titration in Japanese patients with hypertension, to support future clinical development of HJB647

Studieoversikt

Status

Rekruttering

Detaljert beskrivelse

Randomized, placebo-controlled, participant- and investigator-blind study consisting of two parts:

  • Part 1 (SAD part): Single oral dose in healthy participants. Sentinel dosing will be applied in each cohort.
  • Part 2 (MAD part): Multiple oral doses in patients with hypertension. Safety reviews will guide dose escalation and up-titration.

Studietype

Intervensjonell

Registrering (Antatt)

64

Fase

  • Fase 1

Kontakter og plasseringer

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

Studiekontakt

  • Navn: Novartis Pharmaceuticals

Studer Kontakt Backup

Studiesteder

    • Tokyo
      • Sumida Ku, Tokyo, Japan, 1300004
        • Rekruttering
        • Novartis Investigative Site

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

Tar imot friske frivillige

Ja

Beskrivelse

Inclusion Criteria:

  • Japanese healthy participants with elevated blood pressure (Part 1) and patients with mild-to-moderate hypertension (Part 2)
  • Age: 18 to 55 years (Part 1) and 18 to 60 years (Part 2)
  • Body weight:

    • Male: ≥ 50.0 kg
    • Female: ≥ 45.0 kg
  • Body Mass Index (BMI): 18.0 to 30.0 kg/m²
  • Axillary body temperature: 35.0-37.5 °C
  • Heart rate: 50-90 bpm
  • Blood pressure criteria are as follows:

    • Part 1: Healthy Participants with Elevated Blood Pressure Screening: Systolic Blood Pressure (SBP): 120 ≤ SBP ≤ 139 mmHg; Diastolic Blood Pressure (DBP): 60 ≤ DBP ≤ 94 mmHg Baseline (Day -1): SBP: 120 ≤ SBP ≤ 179 mmHg; DBP: 60 ≤ DBP ≤ 109 mmHg
    • Part 2: Patients with Hypertension Screening and Baseline (Day -1): SBP: 140 ≤ SBP ≤ 179 mmHg; DBP: 60 ≤ DBP ≤ 109 mmHg

Exclusion Criteria:

  • Significant illness, including infectious diseases that have not resolved within 30 days prior to baseline
  • History or current diagnosis of ECG or cardiac abnormalities indicating significant risk of safety for participants such as:

    • Concomitant clinically significant cardiac arrhythmias, e.g., sustained ventricular tachycardia, and clinically significant second- or third-degree AV block without a pacemaker.
    • History of familial long QT syndrome or known family history of Torsades de Pointes
    • Resting QT interval corrected by Fridericia's formula (QTcF) ≥ 450 msec (male) or ≥ 460 msec (female) at screening
  • At screening, hypokalemia or hypomagnesemia defined as potassium or magnesium values below the LLN on repeat measurement, or laboratory abnormalities indicating hypothyroidism, as determined at the discretion of the investigator
  • HbA1c ≥ 7.0% or LDL cholesterol ≥ 180 mg/dL or triglycerides ≥ 250 mg/dL
  • Use of any prescription drugs or herbal supplements within 4 weeks prior to initial dosing, and/or OTC medication or dietary supplements (vitamins included) within 2 weeks prior to initial dosing
  • Women of childbearing potential

Other protocol-defined inclusion/exclusion criteria may apply

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: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Part 1-1: HJB647 low dose
Single dose Day 1 in Part 1
HJB647 oral capsule
Eksperimentell: Part 1-2: HJB647 mid-dose
Single dose Day 1 in Part 1
HJB647 oral capsule
Eksperimentell: Part 1-3: HJB647 high dose
Single dose Day 1 in Part 1
HJB647 oral capsule
Placebo komparator: Part 1: Placebo
Single dose Day 1 in Part 1
Matchende oral placebo
Eksperimentell: Part 2-1: HJB647 multiple oral doses
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
HJB647 oral capsule
Eksperimentell: Part 2-2: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
HJB647 oral capsule
Eksperimentell: Part 2-3: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
HJB647 oral capsule
Eksperimentell: Part 2-4: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
HJB647 oral capsule
Eksperimentell: Part 2-5: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
HJB647 oral capsule
Placebo komparator: Part 2: Placebo
Multiple oral doses of placebo with adaptive up-titration in Part 2
Matchende oral placebo

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Part 1: Cmax
Tidsramme: Part 1 on Day 1
Cmax: The maximum (peak) observed plasma, blood, serum, or other body fluid drug concentration after single dose administration (mass x volume-1)
Part 1 on Day 1
Part 1: Tmax
Tidsramme: Part 1 on Day 1
Tmax: The time to reach maximum (peak) plasma, blood, serum, or other body fluid drug concentration after single dose administration (time)
Part 1 on Day 1
Part 1: AUClast
Tidsramme: Part 1 on Day 1
AUClast: The AUC from time zero to the last measurable concentration sampling time (tlast) (mass x time x volume-1)
Part 1 on Day 1
Part 1: AUCinf
Tidsramme: Part 1 on Day 1
AUCinf: The AUC from time zero to infinity (mass x time x volume-1)
Part 1 on Day 1
Part 1: T1/2
Tidsramme: Part 1 on Day 1
T1/2: The elimination half-life associated with the terminal slope (λz) of a semi logarithmic concentration-time curve (time). Use qualifier for other half-lives
Part 1 on Day 1
Part 2: Number of participants with AEs
Tidsramme: Up to 51 days
Number of participants with adverse events (AEs) including abnormal vital signs, ECG, and safety laboratory parameters
Up to 51 days

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Part 2: Cmax
Tidsramme: Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
Cmax: The maximum (peak) observed plasma, blood, serum, or other body fluid drug concentration after single dose administration (mass x volume-1)
Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
Part 2: Tmax
Tidsramme: Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
Tmax: The time to reach maximum (peak) plasma, blood, serum, or other body fluid drug concentration after single dose administration (time)
Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
Part 2: AUClast
Tidsramme: Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
AUClast: The AUC from time zero to the last measurable concentration sampling time (tlast) (mass x time x volume-1)
Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
Part 2: AUCinf
Tidsramme: Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
AUCinf: The AUC from time zero to infinity (mass x time x volume-1)
Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
Part 2: AUCtau
Tidsramme: Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
AUCtau: The AUC calculated to the end of a dosing interval (tau) at steady-state (amount x time x volume-1)
Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
Part 2: T1/2
Tidsramme: Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
T1/2: The elimination half-life associated with the terminal slope (λz) of a semi logarithmic concentration-time curve (time). Use qualifier for other half-lives
Part 2 Day 1, Day 7, Day 8, Day 14, Day 15 and Day 21
Part 1: Number of participants with AEs
Tidsramme: Up to 31 days
Number of participants with adverse events (AEs) including abnormal vital signs, ECG, and safety laboratory parameters
Up to 31 days
Part 2: Office blood pressure change from baseline
Tidsramme: Baseline to Day 27 of part 2
Change in office blood pressure from baseline
Baseline to Day 27 of part 2
Part 2: Heart rate change from baseline
Tidsramme: Baseline to Day 27 of part 2
Change in heart rate from baseline
Baseline to Day 27 of part 2

Samarbeidspartnere og etterforskere

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

Etterforskere

  • Studieleder: Novartis Pharmaceuticals, Novartis Pharmaceuticals

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 (Faktiske)

2. juli 2026

Primær fullføring (Antatt)

25. desember 2026

Studiet fullført (Antatt)

25. desember 2026

Datoer for studieregistrering

Først innsendt

8. juni 2026

Først innsendt som oppfylte QC-kriteriene

8. juni 2026

Først lagt ut (Faktiske)

12. juni 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

22. juli 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

21. juli 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

Novartis is committed to sharing with qualified external researchers, access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations.

This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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