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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
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
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
Inschrijving (Geschat)
Fase
- Fase 1
Contacten en locaties
Studiecontact
- Naam: Novartis Pharmaceuticals
Studie Contact Back-up
- Naam: Novartis Pharmaceuticals
- Telefoonnummer: +81337978748
- E-mail: novartis.email@novartis.com
Studie Locaties
-
-
Tokyo
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Sumida Ku, Tokyo, Japan, 1300004
- Werving
- Novartis Investigative Site
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
Accepteert gezonde vrijwilligers
Beschrijving
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
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Dubbele
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Part 1-1: HJB647 low dose
Single dose Day 1 in Part 1
|
HJB647 oral capsule
|
|
Experimenteel: Part 1-2: HJB647 mid-dose
Single dose Day 1 in Part 1
|
HJB647 oral capsule
|
|
Experimenteel: Part 1-3: HJB647 high dose
Single dose Day 1 in Part 1
|
HJB647 oral capsule
|
|
Placebo-vergelijker: Part 1: Placebo
Single dose Day 1 in Part 1
|
Bijpassende orale placebo
|
|
Experimenteel: Part 2-1: HJB647 multiple oral doses
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
|
HJB647 oral capsule
|
|
Experimenteel: Part 2-2: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
|
HJB647 oral capsule
|
|
Experimenteel: Part 2-3: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
|
HJB647 oral capsule
|
|
Experimenteel: Part 2-4: HJB647 multiple oral doses (optional cohort)
Multiple oral doses of HJB647 with adaptive up-titration in Part 2
|
HJB647 oral capsule
|
|
Experimenteel: 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-vergelijker: Part 2: Placebo
Multiple oral doses of placebo with adaptive up-titration in Part 2
|
Bijpassende orale placebo
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Part 1: Cmax
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: Up to 51 days
|
Number of participants with adverse events (AEs) including abnormal vital signs, ECG, and safety laboratory parameters
|
Up to 51 days
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Part 2: Cmax
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: Baseline to Day 27 of part 2
|
Change in heart rate from baseline
|
Baseline to Day 27 of part 2
|
Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Studie directeur: Novartis Pharmaceuticals, Novartis Pharmaceuticals
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- CHJB647A11101
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
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
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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