New drug aims to curb impulsive behavior in opioid addiction
NCT ID NCT06628622
First seen Jun 24, 2026 · Last updated Jul 31, 2026 · Updated 2 times
Summary
This early-stage trial tests whether a daily tablet called BI 1356225 can improve impulse control in people with opioid use disorder who are already taking buprenorphine. About 60 participants will be randomly assigned to receive either the study drug or a placebo for 8 days. Researchers will measure impulsivity using computer tasks and questionnaires, and monitor safety closely.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- BI 1356225
- What this could lead to
- If it works, this could point toward a new treatment to help people with opioid addiction better control impulses and reduce risky behaviors.
- What could go wrong
- This is a very early Phase 1 trial with only 60 people, so it may not show a clear benefit. The study is also currently suspended, which could indicate challenges.
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
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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12 people
The number who actually took part.
- Started
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Jan 2025
- Finished
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Jul 2026
- 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
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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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: 1. Male and female participants, 18 to 65 years of age, both inclusively, at the time of consent 2. Meet current diagnostic and statistical manual of mental disorders, fifth edition (DSM-5) criteria for opioid use disorder, of at least moderate severity within the 12 months prior to screening 3. Currently engaged in medications for opioid use disorder (MOUD) treatment with one of the following regimens: 1. buprenorphine/naloxone sublingual film total daily dose ranging from 8 mg/2 mg to 24 mg/6 mg for at least 2 weeks at screening OR 2. buprenorphine/naloxone sublingual tablet from 5.7 mg/1.4 mg to 17.1 mg/4.3 mg total daily dose for at least 2 weeks at screening OR 3. buprenorphine sublingual tablet from 8 mg to 24 mg total daily dose for at least 2 weeks at screening OR 4. on depot injectable buprenorphine for at least 5 weeks at screening, with at least 1 week since last depot buprenorphine injection 4. Have a current MOUD prescription in accordance with inclusion criterion 3 and a positive urine drug screen for buprenorphine during screening and upon presenting for randomization to document buprenorphine use 5. Willingness to abstain from using alcohol for 24 hours (h) and all other drugs of abuse for 72 h prior to Day 1 and through discharge from the trial site on Day 9 6. Women of child-bearing potential must be able and willing, as confirmed by the investigator, to use highly effective methods of contraception 7. Further inclusion criteria apply. Exclusion Criteria: 1. Lifetime diagnosis of schizophrenia, schizoaffective disorder, schizophreniform disorder, bipolar I disorder, delusional disorder, or autism spectrum disorder as confirmed by the mini international neuropsychiatric interview (MINI) at the screening visit 2. Moderate or severe substance use disorder other than opioid use disorder (OUD) within the 6 months prior to screening (excluding tobacco, caffeine, and moderate stimulant use) 3. Severe stimulant use disorder within the 3 months prior to screening 4. Any other psychiatric disorder that is not currently stable in symptoms and treatment. Stable is defined as having no significant changes in symptom acuity or treatment (medication or psychotherapy treatment) in the 8 weeks prior to randomization 5. Score of ≥20 on the Montgomery-Åsberg Depression Rating Scale (MADRS) 6. Positive results on a urine drug screen for ≥3 drugs (not counting buprenorphine or TCAs) at screening. In the case of a positive drug screen for 1 or 2 agents, if the participant does not meet the exclusion criteria regarding substance use disorder for these compounds, they may be included if the investigator determines that use will not be an impediment to trial participation or accurate data collection 7. Any positive result on a urine drug screen (not counting buprenorphine, TCAs, or cannabis) at admission to the trial site on Day -1 8. Intoxication at screening or randomization, as determined by clinical exam and breathalyzer 9. Further exclusion criteria apply.
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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
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Collaborative Neuroscience Research, LLC, Los Alamitos
Los Alamitos, California, 90720, United States
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Hassman Research Institute-Marlton-66897
Marlton, New Jersey, 08053, United States
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University of California Los Angeles
Los Angeles, California, 90095, United States
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Virginia Commonwealth University
Richmond, Virginia, 23298, United States
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iResearch Atlanta
Decatur, Georgia, 30030, United States
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Other studies related to the condition(s) this trial covers.
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