New Drug's brain activity measured in tiny early trial
NCT ID NCT07655518
First seen Jun 25, 2026 · Last updated Jul 10, 2026 · Updated 2 times
Summary
This early study tests a new drug called BMS-986521 in 12 healthy adults. Researchers use PET scans to see how much of the drug reaches and attaches to M4 receptors in the brain. The goal is to learn about the drug's action, not to treat any illness. This is a first step before testing in patients with brain disorders.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- BMS-986521
- What this could lead to
- If successful, this study could help researchers understand how BMS-986521 interacts with brain receptors, potentially guiding future treatments for conditions like Alzheimer's or schizophrenia.
- What could go wrong
- This is a very early Phase 1 study with only 12 healthy volunteers. It is designed to measure brain activity, not to treat any disease. The drug may not work as expected or could cause side effects.
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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About 12 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2026
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- 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 55 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Participants must be healthy male and female (as assigned at birth) who are individuals not of childbearing potential (INOCBP) without clinically significant deviation from normal in medical history, PE, 12-lead ECG, and clinical laboratory assessments. * Participants must have a BMI of 18 to 30 kg/m\^2, inclusive, and total body weight ≥ 50 kg. Exclusion Criteria: * Participants must not have presence or history of any clinically relevant abnormality, condition, or disease-CNS, cardiovascular, renal, hepatic, hematologic, GI, endocrine, pulmonary, psychiatric, neurologic (eg, seizure disorder), or immunologic. * Participants must not have history of rhabdomyolysis. * Participants must not have current or recent (within 3 months of study intervention administration) clinically significant GI disease. * Other protocol defined inclusion/exclusion criteria apply.
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Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Universitaire Ziekenhuizen Leuven - Campus Gasthuisberg
RECRUITINGLeuven, 3000, Belgium
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