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- Klinische proef NCT07813663
A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of JZP269 in Healthy Male and Female Participants
4 september 2026 bijgewerkt door: Jazz Pharmaceuticals
A Phase 1, Randomized, Double-Blind, Sponsor-Unblinded, Placebo-Controlled, Single-Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of JZP269 in Healthy Male and Female Participants
This study will characterize the safety, tolerability, pharmacokinetics (PK), and pharmacodynamic (PD) of JZP269 in healthy participants.
Studie Overzicht
Toestand
Nog niet aan het werven
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
This first-in-human study is designed to characterize the safety, tolerability, pharmacokinetics (PK), and pharmacodynamic (PD) of JZP269, an orexin-2 receptor agonist, in healthy participants.
The study will also assess the effect of food on JZP269 PK, characterize cerebrospinal fluid (CSF) exposure, and evaluate the wake-promoting PD effects using the Maintenance of Wakefulness Test (MWT) and Karolinska Sleepiness Scale (KSS) in sleep-deprived participants.
Studietype
Ingrijpend
Inschrijving (Geschat)
188
Fase
- Fase 1
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studiecontact
- Naam: Clinical Trial Disclosure & Transparency
- Telefoonnummer: 215-832-3750
- E-mail: ClinicalTrialDisclosure@JazzPharma.com
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
Accepteert gezonde vrijwilligers
Ja
Beschrijving
Participants are eligible to be included in the study only if all of the following criteria apply:
- Is 18 to 55 years of age, inclusive, at the time of signing the informed consent.
- Is overtly healthy as determined by medical evaluation, including medical history, physical examination, laboratory tests, and cardiac/blood pressure monitoring.
- Has a body weight of at least 45 kg and BMI within the range of 18.5 to 30 kg/m^2 (inclusive).
Participants are excluded from the study if any of the following criteria apply:
- Has a history of or presence of clinically significant medical illness as specified in the protocol.
- Has a family history (first degree relative) of torsades de pointes, premature sudden death, long QT syndrome, or clinically significant cardiac conduction disorders.
- Has a known or suspected history of schizophrenia or other psychotic illness or a history of severe personality disorder or other significant psychiatric disorder.
- Has a history (within 5 past years) or presence of diagnosis of alcohol abuse or alcohol use disorder, substance abuse or substance use disorder, or known drug dependence or is seeking treatment for an alcohol or substance abuse related disorder.
- Has a current diagnosis of or is receiving treatment for depression or has a history (within past 5 years) of clinically significant major depressive episode.
- Has a history of suicide attempt, a current suicidal risk as determined from history, or the presence of active suicidal ideation as indicated by a positive response to Item 4 or Item 5 on the C-SSRS (within the past 24 months).
- In participants where cerebrospinal fluid will be collected, any contraindications to lumbar puncture including increased intracranial pressure, conditions that may lead to brain herniation, a history of degenerative spine disease or lumbar spinal stenosis, a history of lumbar surgery, or prior history of adverse experience with lumbar puncture (eg, headache).
- Has a clinically significant ECG abnormality per investigator assessment or an average PR > 200 msec, average QRS > 110 msec, average QTcF > 440 msec for men and women, or flattened or difficult to distinguish T-waves.
- Has a resting supine systolic blood pressure > 140 mmHg or < 90 mmHg, resting supine diastolic blood pressure > 90 mmHg or < 50 mmHg, or resting supine heart rate > 100 bpm or < 40 bpm at screening or check-in.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
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: JZP269
Participants will receive JZP269.
|
Administered as described.
|
|
Placebo-vergelijker: Placebo
Participants will receive a matching placebo.
|
Administered as described.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Number of Participants Reporting Treatment-emergent Adverse Events
Tijdsspanne: Day 1 of dosing and monitoring period up to 7 days after last dose (Safety Follow Up Visit)
|
Day 1 of dosing and monitoring period up to 7 days after last dose (Safety Follow Up Visit)
|
|
|
Pharmacokinetic Parameter Maximum Concentration (Cmax) of JZP269
Tijdsspanne: Predose up to 48 hours postdose
|
Predose up to 48 hours postdose
|
|
|
Pharmacokinetic Parameter Time to Maximum Concentration (Tmax) of JZP269
Tijdsspanne: Predose up to 48 hours postdose
|
Predose up to 48 hours postdose
|
|
|
Pharmacokinetic Parameter Apparent Terminal Elimination Half-life (t1/2) of JZP269
Tijdsspanne: Predose up to 48 hours postdose
|
Predose up to 48 hours postdose
|
|
|
Pharmacokinetic Parameter Area Under the Concentration-Time Curve (AUC) of JZP269
Tijdsspanne: Predose up to 48 hours postdose
|
Area under the concentration-time curve from time 0 to 24 hours (AUC0-24), area under the concentration time curve from time 0 to the last measurable concentration (AUC0-last), and area under the concentration-time curve from time 0 to infinity will be assessed (AUC∞).
|
Predose up to 48 hours postdose
|
|
Pharmacokinetic Parameter Oral Clearance (CL/F) of JZP269
Tijdsspanne: Predose up to 48 hours postdose
|
Predose up to 48 hours postdose
|
|
|
Pharmacokinetic Parameter Apparent Volume of Distribution During the Terminal Phase (Vz/F) of JZP269
Tijdsspanne: Predose up to 48 hours postdose
|
Predose up to 48 hours postdose
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Dose Proportionality of JZP269 Area Under the Concentration-Time Curve (AUC)
Tijdsspanne: Predose up to 48 hours postdose
|
Dose proportionality of JZP269 AUC0-last, AUC∞, and AUC0-24 will be assessed.
|
Predose up to 48 hours postdose
|
|
Dose Proportionality of JZP269 Maximum Concentration (Cmax)
Tijdsspanne: Predose up to 48 hours postdose
|
Predose up to 48 hours postdose
|
|
|
The Effect of Food on the PK of JZP269 Cmax
Tijdsspanne: Predose up to 48 hours postdose
|
The effect of food on the PK of JZP269 relative to that observed in the fasted state will be assessed.
|
Predose up to 48 hours postdose
|
|
The Effect of Food on the PK of JZP269 Tmax
Tijdsspanne: Predose up to 48 hours postdose
|
The effect of food on the PK of JZP269 relative to that observed in the fasted state will be assessed.
|
Predose up to 48 hours postdose
|
|
The Effect of Food on the PK of JZP269 t1/2
Tijdsspanne: Predose up to 48 hours postdose
|
The effect of food on the PK of JZP269 relative to that observed in the fasted state will be assessed.
|
Predose up to 48 hours postdose
|
|
The Effect of Food on the PK of JZP269 AUC
Tijdsspanne: Predose up to 48 hours postdose
|
The effect of food on the PK of JZP269 relative to that observed in the fasted state will be assessed.
|
Predose up to 48 hours postdose
|
|
Mean Concentrations of JZP269 in Cerebrospinal Fluid
Tijdsspanne: Predose up to 48 hours postdose
|
Predose up to 48 hours postdose
|
|
|
Mean Sleep Latency on the Maintenance of Wakefulness Test (MWT) in Sleep-deprived Participants
Tijdsspanne: Day 1 of dosing and monitoring period
|
The MWT measures a participant's ability to remain awake under quiet conditions during the day.
Sleep latency is the time it takes for a participant to fall asleep while trying to remain awake during the MWT, and sleep onset is determined objectively by electroencephalography.
The MWT calculates mean sleep latency as the average time to sleep onset.
Shorter mean sleep latency indicates a greater difficulty maintaining wakefulness.
|
Day 1 of dosing and monitoring period
|
|
Mean Karolinska Sleepiness Scale (KSS) Score in Sleep-deprived Participants
Tijdsspanne: Day 1 of dosing and monitoring period
|
The KSS is a 9-point scale that measures subjective sleepiness during the preceding 10 minutes, ranging from 1 ("extremely alert") to 9 ("very sleepy, great effort to keep awake, fighting sleep").
Higher scores indicate greater sleepiness.
|
Day 1 of dosing and monitoring period
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Medewerkers
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Geschat)
22 september 2026
Primaire voltooiing (Geschat)
27 februari 2027
Studie voltooiing (Geschat)
27 februari 2027
Studieregistratiedata
Eerst ingediend
4 september 2026
Eerst ingediend dat voldeed aan de QC-criteria
4 september 2026
Eerst geplaatst (Werkelijk)
10 september 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
10 september 2026
Laatste update ingediend die voldeed aan QC-criteria
4 september 2026
Laatst geverifieerd
1 september 2026
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Andere studie-ID-nummers
- JZP269-101
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
JA
Beschrijving IPD-plan
In accordance with ICMJE requirements, Jazz Pharmaceuticals may provide qualified external researchers access to individual participant data (IPD) and clinical trial data that underlie the results of this trial upon request.
Qualified researchers can submit a request on https://www.jazzpharma.com/science/clinical-trial-data-sharing/
as outlined.
Jazz Pharmaceuticals reserves the right not to consider a request.
For inquiries about Jazz's data sharing policy contact clinicaldatasharing@jazzpharma.com.
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Ja
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
product vervaardigd in en geëxporteerd uit de V.S.
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .