A Study of Elenestinib in Healthy Adult Female Participants
Completed · Phase 1
Conditions studied: Healthy Participants
In brief
The main objectives of this study are to determine the effect of elenestinib on the pharmacokinetic parameters (how the drug is absorbed, distributed, and processed by the body) of midazolam, and to determine the effect of elenestinib on the pharmacokinetic parameters of levonorgestrel/ethinyl estradiol, when given as a combined oral contraceptive. Healthy adult participants will receive midazolam and levonorgestrel/ethinyl estradiol with and without elenestinib and have blood samples taken.
Key facts
- Study ID
- NCT07388511
- Run by
- Blueprint Medicines Corporation
- People needed
- 20
- Starts
- 2026-02-05
- Expected to finish
- 2026-04-02
- Last updated by the study team
- 2026-04-20
Who can join
Age: 18 and older, up to 65. Sex: female. Healthy volunteers: accepted.
Where it is running
- Celerion, Inc — Tempe, Arizona, United States
Full record on ClinicalTrials.gov
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