- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07644364
HJB647 Phase 1b Study in Japanese Healthy Participants With Elevated Blood Pressure and Patients With Hypertension
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
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
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.
Studientyp
Einschreibung (Geschätzt)
Phase
- Phase 1
Kontakte und Standorte
Studienkontakt
- Name: Novartis Pharmaceuticals
Studieren Sie die Kontaktsicherung
- Name: Novartis Pharmaceuticals
- Telefonnummer: +81337978748
- E-Mail: novartis.email@novartis.com
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Beschreibung
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
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Doppelt
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Part 1-1: HJB647 low dose
Single dose Day 1 in Part 1
|
HJB647 oral capsule
|
|
Experimental: Part 1-2: HJB647 mid-dose
Single dose Day 1 in Part 1
|
HJB647 oral capsule
|
|
Experimental: 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
|
Passendes orales Placebo
|
|
Experimental: Part 2-1: HJB647 multiple oral doses
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
|
HJB647 oral capsule
|
|
Experimental: Part 2-2: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
|
HJB647 oral capsule
|
|
Experimental: Part 2-3: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
|
HJB647 oral capsule
|
|
Experimental: Part 2-4: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
|
HJB647 oral capsule
|
|
Experimental: 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
|
Passendes orales Placebo
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Part 1: Cmax
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: Up to 51 days
|
Number of participants with adverse events (AEs) including abnormal vital signs, ECG, and safety laboratory parameters
|
Up to 51 days
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Part 1: Number of participants with AEs
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: Baseline to Day 27 of part 2
|
Baseline to Day 27 of part 2
|
|
|
Part 2: Heart rate change from baseline
Zeitfenster: Baseline to Day 27 of part 2
|
Baseline to Day 27 of part 2
|
|
|
Part 2: Change in 24-hr mean SBP/DBP
Zeitfenster: 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
Zeitfenster: 27 days
|
Daytime mean BP, and nighttime mean BP (ambulatory blood pressure monitoring)
|
27 days
|
Mitarbeiter und Ermittler
Sponsor
Ermittler
- Studienleiter: Novartis Pharmaceuticals, Novartis Pharmaceuticals
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- CHJB647A11101
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Beschreibung des IPD-Plans
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
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
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