A Study to Evaluate the Safety and Efficacy of Relugolix in Men With Advanced Prostate Cancer

Completed · Phase 3

Conditions studied: Prostate Cancer

In brief

The purpose of this study is to determine the efficacy and safety of relugolix 120 milligrams (mg) orally once daily for 48 weeks on maintaining serum testosterone suppression to castrate levels (\< 50 nanograms/deciliter \[ng/dL\]) in participants with androgen-sensitive advanced prostate cancer.

Key facts

Study ID
NCT03085095
Run by
Myovant Sciences GmbH
People needed
1134
Starts
2017-04-18
Expected to finish
2021-11-26
Last updated by the study team
2022-01-18

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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