Clinical Trials Directory

Trials / Completed

CompletedNCT02655237

A Phase 3 Study to Evaluate the Efficacy and Safety of Relugolix (TAK-385) 40 mg Compared With Leuprorelin in the Treatment of Uterine Fibroids

A Multicenter, Randomized, Double-Blind, Parallel-Group, Phase 3 Study to Evaluate the Efficacy and Safety of Oral TAK-385 40 mg Compared With Leuprorelin in the Treatment of Uterine Fibroids

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
281 (actual)
Sponsor
Takeda · Industry
Sex
Female
Age
20 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the efficacy of Relugolix (TAK-385) 40 mg administered orally once daily for 12 weeks, compared with leuprorelin injection (once every 4 weeks, 1.88 mg or 3.75 mg subcutaneously \[SC\]/time) in patients with uterine fibroids.

Detailed description

The drug tested in this study was called Relugolix (TAK-385). Relugolix was tested to treat people who had uterine fibroids. The study enrolled 281 patients. Participants received relugolix placebo and leuprorelin acetate placebo in run in period for 3 to 6 weeks. After run-in period, participants were randomly assigned (by chance, like flipping a coin) to one of the two treatment groups in 1:1 ratio: * Relugolix 40 mg * Leuprorelin 1.88 or 3.75 mg Participants received relugolix tablets once daily along with leuprorelin 1.88 mg or 3.75 mg subcutaneous injection once in 4 weeks for 24 weeks in treatment period. This multi-center trial was conducted in Japan. The overall time to participate in this study was approximately 32 to 40 weeks including run-in period of 3 to 6 weeks and a treatment period of 24 weeks. Participants will make multiple visits to the clinic, and a final visit 4 weeks after last dose of study drug for a follow-up assessment.

Conditions

Interventions

TypeNameDescription
DRUGRelugolixRelugolix tablets
DRUGRelugolix PlaceboRelugolix placebo-matching tablets
DRUGLeuprorelinLeuprorelin injection
DRUGLeuprorelin PlaceboLeuprorelin placebo-matching injections

Timeline

Start date
2016-03-05
Primary completion
2017-05-17
Completion
2017-09-25
First posted
2016-01-13
Last updated
2019-03-22
Results posted
2019-03-22

Locations

25 sites across 1 country: Japan

Source: ClinicalTrials.gov record NCT02655237. Inclusion in this directory is not an endorsement.