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RECRUITING
NCT07502417
PHASE1
A Phase 1 Study to Assess the Effect of ABBV-722 on Ethinyl Estradiol and Levonorgestrel Drug Levels in Healthy Adult Female Participants
Sponsor: AbbVie
View on ClinicalTrials.gov
Summary
The objective of this study is to assess the effect of repeated doses of ABBV-722 on the single dose pharmacokinetics (PK) of ethinyl estradiol and levonorgestrel.
Official title: A Phase 1 Study to Assess the Effect of Multiple Doses of ABBV-722 on the Pharmacokinetics of a Combined Oral Contraceptive Containing Ethinyl Estradiol and Levonorgestrel
Key Details
Gender
FEMALE
Age Range
18 Years - 65 Years
Study Type
INTERVENTIONAL
Enrollment
16
Start Date
2026-03-25
Completion Date
2026-07
Last Updated
2026-03-31
Healthy Volunteers
Yes
Conditions
Interventions
DRUG
Ethinyl Estradiol + Levonorgestrel
Oral
DRUG
ABBV-722
Oral
Locations (1)
Acpru /Id# 281745
Grayslake, Illinois, United States