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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

Interventions

DRUG

Ethinyl Estradiol + Levonorgestrel

Oral

DRUG

ABBV-722

Oral

Locations (1)

Acpru /Id# 281745

Grayslake, Illinois, United States