A Mass Balance Study of Oral [14C] ABBV-932 in Healthy Adult Male Participants
NCT ID: NCT06953934
Last Updated: 2025-08-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
PHASE1
8 participants
INTERVENTIONAL
2025-10-14
2026-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
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ABBV-932
Participants will receive a single oral dose of ABBV-932 on day 1.
ABBV-932
Oral Capsule
Interventions
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ABBV-932
Oral Capsule
Eligibility Criteria
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Inclusion Criteria
* Male participant who is not considering fathering a child or donating sperm during the study and for 100 days after the study drug administration
* A condition of general good health, based upon the results of a medical history, physical exam
Exclusion Criteria
* Use of any medications/products known to alter drug absorption, metabolism, or excretion processes, within 30 days or within a period defined by 5 half-lives, whichever is longer, prior to study drug administration.
* Prior exposure to ABBV-932 or cariprazine within the past 90 days.
18 Years
65 Years
MALE
Yes
Sponsors
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AbbVie
INDUSTRY
Responsible Party
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Principal Investigators
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ABBVIE INC.
Role: STUDY_DIRECTOR
AbbVie
Central Contacts
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Related Links
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Other Identifiers
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M24-991
Identifier Type: -
Identifier Source: org_study_id
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