Study of Single Doses of HBS-104 in Acutely Sleep-deprived Healthy Participants
Harmony Biosciences Management, Inc. · NCT07848659
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–55 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 1
- Target enrollment
- 12
- US sites recruiting
- 1
- Study start
- August 28, 2026
- Record last updated
- September 30, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This is a study to evaluate the pharmacodynamic effects, safety, tolerability, and pharmacokinetics of HBS-104 in acutely sleep-deprived healthy adult participants.
Being studied: HBS-104; Placebo
Conditions: Sleep Deprivation
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Provide written informed consent before any study-related procedures are performed.
- Be healthy as determined by assessments at the Screening Visit.
Exclusion Criteria
- Female with a positive pregnancy test at Screening Visit or upon check-in for Period 1.
- Is currently breastfeeding or planning to breastfeed over the course of the study. Lactating women must agree not to breastfeed for the duration of the study and for 7 days after their final dose of study drug.
Note: Additional inclusion/exclusion criteria may apply, per protocol
Recruiting US locations
Sponsor Clinical Site - New Jersey
Eatontown, NJ 07724
Study contacts (from the official record)
- Clinical Trials Administrator · see email · clinicaltrials@harmonybiosciences.com
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