A Study to Investigate The Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of JZP441 in Sleep-deprived Healthy Participants
- Registration Number
- NCT05651152
- Lead Sponsor
- Jazz Pharmaceuticals
- Brief Summary
This Phase 1, double-blind, randomized, placebo-controlled study will characterize the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of ascending nighttime doses of JZP441 in sleep-deprived healthy participants.
- Detailed Description
This study will initially employ nighttime dosing in sleep-deprived healthy participants. Participants (up to 12 per cohort) will be randomized to study intervention. Participants will remain awake during the day and then will be dosed at night. Safety, tolerability, PK and PD assessments will be conducted for nighttime dose.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 105
Inclusion Criteria
- 18 to 50 years of age inclusive, at the time of signing the informed consent
- Are overtly healthy as determined by medical evaluation, including medical history, physical exam, laboratory tests, and cardiac/blood pressure monitoring
Exclusion Criteria
- Female participants who are pregnant, nursing, or lactating
- History or presence of clinically significant allergy or allergy to band aids, adhesive dressing, electrocardiogram (ECG) patches, or medical tape
- History or presence of gastrointestinal (including prior bariatric bypass surgery), hepatic or renal disease, or any other condition that may interfere with absorption, distribution, metabolism, or excretion of drugs
- Presence of renal impairment or calculated creatinine clearance < 80 mL/min
- Triplicate 12-lead ECG demonstrating a mean QTcF > 450 msec for males and > 470 msec for females or any other clinically significant ECG abnormality per investigator assessment at Screening or Day -1
- Presence or history of significant cardiovascular disease including but not limited to: myocardial infarction, uncontrolled hypertension, systolic blood pressure > 140 mmHg or diastolic blood pressure > 90 mmHg (at Screening or Day -1), angina pectoris, clinically significant arrhythmias, clinically significant valvular heart disease, history of any revascularization procedures or second or third-degree heart block with/without a pacemaker, heart failure, or family history of Torsades de Pointes
- Laboratory value(s) outside the laboratory reference range that are considered to be clinically significant by the investigator
- Current diagnosis of or receiving treatment for depression; past (within 5 years) major depressive episode according to Diagnostic and Statistical Manual of Mental Disorders-5 (DSM-5) criteria; history of suicide attempt, current suicidal risk as determined from history, or presence of active suicidal ideation
- History or presence of bipolar disorder, bipolar related disorders, schizophrenia, schizophrenia spectrum disorders, or other psychotic disorders according to DSM-5 criteria
- Participation in another clinical study of an investigational drug or medical device within 30 days or 5 half-lives (whichever is longer) prior to check-in on Day -1
- Presence at Screening of human immunodeficiency virus (HIV) antibody, hepatitis B surface antigen, hepatitis C antibody, or a clinical history of these infections
- History of chronic insomnia (as defined by DSM-5 criteria)
- Has been diagnosed with sleep apnea or been identified as being at high risk for sleep apnea by standardized questionnaire (STOP-BANG)
- Any clinically relevant medical, behavioral, or psychiatric disorder that is associated with excessive sleepiness
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description JZP441 JZP441 Participants who will be randomized to receive an oral dose of JZP441. Placebo Placebo Participants who will be randomized to receive an oral dose of placebo.
- Primary Outcome Measures
Name Time Method Number of Participants With Treatment-emergent Adverse Events After Administration of JZP441 in Sleep-deprived Healthy Participants 1 hour postdose up to Day 8
- Secondary Outcome Measures
Name Time Method Pharmacokinetic Parameter Area Under the Concentration-Time Curve (AUC) of JZP441 Pre-dose and multiple post-dose timepoints, up to 36 hours Pharmacokinetic Parameter Maximum Plasma Concentration (Cmax) Levels of JZP441 Pre-dose and multiple post-dose timepoints, up to 36 hours Pharmacokinetic Parameter Time to Maximum Plasma Concentration (Tmax) of JZP441 Pre-dose and multiple post-dose timepoints, up to 36 hours
Trial Locations
- Locations (2)
Clinical Site 1
🇺🇸Eatontown, New Jersey, United States
Clinical Site 2
🇺🇸New York, New York, United States