New sleep drug shows promise in early trial
NCT ID NCT06956495
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a new drug called tasipimidine can help people with insomnia fall asleep faster and stay asleep longer. 190 adults with chronic insomnia took either the drug or a placebo for 3 nights in a sleep clinic, with some continuing for 4 more weeks at home. Researchers measured sleep quality using brain-wave recordings and sleep diaries to see if the drug works better than a dummy pill.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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190 people
The number who actually took part.
- Started
-
Aug 2023
- Finished
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Sep 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 65 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Signed informed consent (IC) for participation in the study. * Male or female subjects with age between 18 and 65 years. * Insomnia disorder * Self-reported history of the following on at least 3 nights per week and for at least 3 months prior to the screening: ≥ 30 minutes to fall asleep, subjective total sleep time ≤ 6 hours. * Insomnia Severity Index© (ISI©) score ≥ 15 in Part 1 and ≥ 11 in Part 2. * Usual bedtime between 21:00 and 02:00. * Regular time in bed between 6 and 9 hours. * Meeting predefined sleep parameter criteria in sleep recording on the 2 screening nights. * Highly effective contraception. Exclusion Criteria: * Body mass index below 18.5 or above 40.0 kg/m2. * Daytime napping ≥ 1 hour per day, and ≥ 3 days per week. * Shift work within 2 weeks prior to the screening visit, or planned shift work during the study. * Travel across ≥ 3 time zones within 2 weeks prior to the screening visit, or planned travel across ≥ 3 time zones during the study. * Use of certain medications affecting central nervous system, e.g. sedatives or stimulans. * Start of other new chronic medication within 14 days prior screening nights and planned change to an ongoing chronic medication during the study. * Cognitive behavioural therapy (CBT) is allowed if the CBT started at least 1 month prior to the 1st screening night and the subject agreed to continue the CBT throughout the study. * Diagnosed sleep-related breathing disorder, including chronic obstructive pulmonary disease and sleep apnoea. * Acute or unstable psychiatric conditions. * Alcohol or substance use disorder within 2 years prior to the screening visit or inability to refrain from drinking alcohol for at least 3 consecutive days. * Significant cardiac disease. * Significant postural hypotension. * Heavy tobacco or other nicotine containing product use. * Caffeine consumption ≥ 600 mg per day or regular caffeine consumption after 4 p.m. * Heart rate \< 50 bpm or \> 100 bpm. * Systolic blood pressure \< 100 or \> 160 mmHg or diastolic blood pressure \< 50 or \> 100 mmHg * Abnormal 12-lead ECG finding. * Significant abnormal laboratory findings including positive drug screen and presence of alcohol in breath test. * Pre-planned elective surgery. * Pregnant or lactating females. * Blood donation or loss of significant amount of blood prior to the study. * Participation in a drug study within 60 days prior to the study. * Restless legs syndrome, circadian rhythm disorder, REM behaviour disorder, or narcolepsy.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Terveystalo Helsinki Uniklinikka
Helsinki, 00380, Finland
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Other studies related to the condition(s) this trial covers.
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