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Assessment of the Relative Bioavailability of ABBV-932 Formulations in Healthy Adult Subjects
This study will assess the relative bioavailability and effect of food on pharmacokinetics of ABBV-932 oral administration in healthy adult participants.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
Yes
Acpru /Id# 266649
Grayslake, Illinois, United States
Start Date
February 26, 2025
Primary Completion Date
March 1, 2026
Completion Date
March 1, 2026
Last Updated
February 24, 2026
9
ACTUAL participants
ABBV-932
DRUG
ABBV-932
DRUG
Lead Sponsor
AbbVie
NCT07310264
NCT00090662
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06342713