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New sleep drug shows promise in early trial

NCT ID NCT06956495

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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.

This is an AI summary of the original study and may miss details. Read our disclaimer.

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

190 people

The number who actually took part.

Started

Aug 2023

Finished

Sep 2025

Lead sponsor

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

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

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

More trials for these conditions

Other studies related to the condition(s) this trial covers.