A Study to Assess Adverse Events and How Oral ABBV-932 Moves Through the Body When Given With Oral Itraconazole in Adult Participants With Bipolar Disorder
Part of paid clinical trials in Los Alamitos, California.
- Sponsor
- AbbVie
- Study ID
- NCT07071532
- Phase
- PHASE1
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Not accepted
Interventions
- ABBV-932 — DRUGOral Capsule
- Itraconazole — DRUGOral Capsule
Study Details
This study will assess the adverse events and how oral ABBV-932 moves through the body when given with oral Itraconazole in adult participants with bipolar disorder.
Key Dates
- First listed
- Jul 17, 2025
- Start date
- Aug 20, 2026
- Status verified
- Sep 2026
- Primary completion
- Feb 28, 2027
- Completion
- Feb 28, 2027
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- BASIC_SCIENCE
Arms
- Experimental: ABBV-932 with ItraconazoleParticipants will receive ABBV-932 in Period 1 followed by Itraconalzole in combination with ABBV-932 in Period 2.
Primary Outcome Measure
Maximum Plasma Concentration (Cmax) of ABBV-932 and active metabolites DCAR and DDCAR [ Time Frame: Up to approximately 29 days ]
Central Contacts
- ABBVIE CALL CENTER844-663-3742
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| CenExel Collaborative Neuroscience Research /ID# 282784 | Los Alamitos | California | 90720 | - |
| Acpru /Id# 276951 | Grayslake | Illinois | 60030 | - |
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