Overview

A Study of Lanabecestat in Healthy Female Participants Taking Oral Contraceptive

Status:
Withdrawn
Trial end date:
2018-10-01
Target enrollment:
Participant gender:
Summary
The study will evaluate the effect of oral contraceptive (birth control pill) on the blood level of lanabecestat when both are given together. Side effects will be monitored and documented. This study will last up to 27 days for each participant, not including screening. Screening is required within 42 days prior to first dose.
Phase:
Phase 1
Details
Lead Sponsor:
Eli Lilly and Company
Collaborator:
AstraZeneca
Treatments:
Contraceptive Agents
Contraceptives, Oral
Estradiol
Estradiol 17 beta-cypionate
Estradiol 3-benzoate
Estradiol valerate
Ethinyl Estradiol
Ethinyl estradiol, levonorgestrel drug combination
Levonorgestrel
Polyestradiol phosphate