A Study to Assess the Adverse Events and How Bretisilocin Intramuscular Injection Moves Through the Body of Healthy Adult Participants
Part of paid clinical trials in Los Alamitos, California.
- Sponsor
- AbbVie
- Study ID
- NCT07604558
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Healthy Volunteer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Accepted
Interventions
- Bretisilocin — DRUGIntramuscular Injection
Study Details
This study will assess the adverse events, tolerability, and how bretisilocin intramuscular (IM) Injection moves through the body of healthy adult Japanese, Han Chinese, and Non-Asian volunteers participants.
Key Dates
- Start date
- May 26, 2026
- Status verified
- Jun 2026
- Primary completion
- Sep 30, 2026
- Completion
- Sep 30, 2026
Study Design
- Enrollment
- 26 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- BASIC_SCIENCE
Arms
- Experimental: Group 1-Bretisilocin-JapaneseParticipants will receive bretisilocin intramuscular (IM) injection on day 1.
- Experimental: Group 1-Bretisilocin-Han ChineseParticipants will receive bretisilocin intramuscular (IM) injection on day 1.
- Experimental: Group 1-Bretisilocin-Non-AsianParticipants will receive bretisilocin intramuscular (IM) injection on day 1.
Primary Outcome Measure
Number of Participants Experiencing Adverse Events [ Time Frame: Up to approximately 32 days ]
Central Contacts
- ABBVIE CALL CENTER844-663-3742
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| CenExel Collaborative Neuroscience Research /ID# 281612 | Los Alamitos | California | 90720 | - |
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