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NCT07328594 · ClinicalTrials.gov registry record · Phase 4
Impact of Daridorexant on Sleep, Daytime Alertness, and Smoking
A Phase 4 study, sponsored by Legacy Health System.
- Not yet
- Registry status
- Phase 4
- Development phase
- 44
- Enrollment target
NCT07328594 is a Phase 4 study that has not yet begun recruiting, run by Legacy Health System. The registered enrollment target is 44 participants.
The verdict
NCT07328594, a Phase 4 study, has not yet begun recruiting, sponsored by Legacy Health System.
- NOT YET RECRUITING
- Registry status
- Phase 4
- Development phase
- 44 participants
- Enrollment target
Study Summary
Tobacco use is the leading cause of preventable death in the U.S., with 480,000 deaths per year and 7.7 million deaths globally. A major clinical symptom associated with abstinence from both licit and illicit drugs is insomnia, which is a clinically verified, major risk factor for relapse. Roughly half of the 40 million smokers in the U.S. attempt to quit annually, with very low rates of success. One major hurdle is poor sleep quality during abstinence. Compounding the problem is that some pharmaceuticals to help reduce smoking can increase insomnia. Poor sleep is recognized as a major impediment to maintaining abstinence from several drugs of abuse, including nicotine. Blockers of orexin have recently been proposed as a promising therapy for smoking cessation. Insomnia has been reported in up to 40% of smokers, and 80% report regular sleep disturbances, which can be amplified during abstinence. A new orexin blocker, daridorexant, was FDA approved within the past two years for the treatment of insomnia, and while it has been tested in healthy individuals with insomnia, it has not been tested in smokers, who suffer from insomnia, particularly during the withdrawal phase when trying to quit. Daridorexant has an improved profile of beneficial effects for those with insomnia, the most notable advantage being its shorter duration of action that promotes daytime alertness, which is problematic for both active smokers and smokers during withdrawal. Poor sleep leads to daytime sleepiness, which often leads to smoking to maintain alertness.
Interventions
- OTHER Placebo
- DRUG Daridorexant 50 mg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 44 participants |
| Start Date | 2026-02-10 |
| Est. Completion | 2027-09-30 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07328594
The ClinicalTrials.gov registry entry for NCT07328594 describes a study currently listed as not yet recruiting, categorized as Phase 4. The registered enrollment target is 44 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Legacy Health System, which has 21 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT07328594 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT07328594 about?
NCT07328594 is a clinical study titled "Impact of Daridorexant on Sleep, Daytime Alertness, and Smoking". Tobacco use is the leading cause of preventable death in the U.S., with 480,000 deaths per year and 7.7 million deaths globally. A major clinical symptom associated with abstinence from both licit and illicit drugs is insomnia, which is a clinically verified, major risk factor for relapse. Roughly h...
What is the current status of trial NCT07328594?
This trial is currently not yet recruiting. It is a Phase 4 study. The enrollment target is 44 participants. The study started on 2026-02-10. Estimated completion is 2027-09-30.
What interventions are being tested in trial NCT07328594?
The interventions under investigation include: Placebo (OTHER), Daridorexant 50 mg (DRUG).
Who is sponsoring clinical trial NCT07328594?
This trial is sponsored by Legacy Health System, which has 21 total clinical trials registered on ClinicalTrials.gov.
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