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

8. juni 2026 opdateret af: 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

Studieoversigt

Status

Ikke rekrutterer endnu

Intervention / Behandling

Detaljeret 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.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

74

Fase

  • Fase 1

Kontakter og lokationer

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

Studiekontakt

  • Navn: Novartis Pharmaceuticals

Undersøgelse Kontakt Backup

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

Tager imod sunde 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

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: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Part 1-1: HJB647 low dose
Single dose Day 1 in Part 1
HJB647 oral capsule
Eksperimentel: Part 1-2: HJB647 mid-dose
Single dose Day 1 in Part 1
HJB647 oral capsule
Eksperimentel: 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
Eksperimentel: Part 2-1: HJB647 multiple oral doses
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
HJB647 oral capsule
Eksperimentel: Part 2-2: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
HJB647 oral capsule
Eksperimentel: Part 2-3: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
HJB647 oral capsule
Eksperimentel: Part 2-4: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
HJB647 oral capsule
Eksperimentel: 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

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
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: AUCtau
Tidsramme: Part 1 on Day 1
AUCtau: The AUC calculated to the end of a dosing interval (tau) at steady-state (amount 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
Foranstaltningsbeskrivelse
Tidsramme
Part 1: Number of participants with AEs
Tidsramme: Up to 27 days
Number of participants with adverse events (AEs) including abnormal vital signs, ECG, and safety laboratory parameters
Up to 27 days
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 2: Office blood pressure change from baseline
Tidsramme: Baseline to Day 27 of part 2
Baseline to Day 27 of part 2
Part 2: Heart rate change from baseline
Tidsramme: Baseline to Day 27 of part 2
Baseline to Day 27 of part 2
Part 2: Change in 24-hr mean SBP/DBP
Tidsramme: Part 2 Day 1, Day 7, Day 8, Day 14, Day 15, Day 21 and Day 22
Change in 24-hr mean Systolic Blood Pressure (SBP)/Diastolic Blood Pressure (DBP), daytime and night time mean Blood Pressure (BP)
Part 2 Day 1, Day 7, Day 8, Day 14, Day 15, Day 21 and Day 22
Part 2: Mean Blood Pressure
Tidsramme: 27 days
Daytime mean BP, and nighttime mean BP (ambulatory blood pressure monitoring)
27 days

Samarbejdspartnere og efterforskere

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

Efterforskere

  • Studieleder: Novartis Pharmaceuticals, Novartis Pharmaceuticals

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)

23. juni 2026

Primær færdiggørelse (Anslået)

20. januar 2027

Studieafslutning (Anslået)

20. januar 2027

Datoer for studieregistrering

Først indsendt

8. juni 2026

Først indsendt, der opfyldte QC-kriterier

8. juni 2026

Først opslået (Faktiske)

12. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

12. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

8. juni 2026

Sidst verificeret

1. maj 2026

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

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

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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