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Clinical Trial Summary

The purpose of this study is to assess the contraceptive efficacy of relugolix combination therapy.


Clinical Trial Description

This is a single-arm, open-label, phase 3 study to assess the contraceptive efficacy of relugolix combination therapy (relugolix 40 milligrams [mg], estradiol [E2] 1 mg, and norethindrone acetate [NETA] 0.5 mg). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04756037
Study type Interventional
Source Sumitomo Pharma Switzerland GmbH
Contact
Status Active, not recruiting
Phase Phase 3
Start date March 18, 2021
Completion date February 2026

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