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Bay1002670, Fibroids, Safety and Efficacy EU,US,Can, Jap — ASTEROID 1  

Leiomyoma Clinical Trial

Official title:
A Randomized, Parallel-group, Double-blind, Placebo Controlled, Multi-center Study to Assess the Efficacy and Safety of Different Doses of BAY1002670 in Subjects With Uterine Fibroids Over 3 Months

Clinical Trial Summary

The study is performed to assess the efficacy and safety of different doses of BAY1002670 in subjects with uterine fibroids. The dose-response relationship will be evaluated. Further, the study aims to establish a population pharmacokinetic/pharmacodynamic relationship for BAY1002670 in subjects with uterine fibroids. To assess the efficacy of BAY1002670 the interchangeability of menstrual pictogram and alkaline hematin method for the judgement of menstrual blood loss will be assessed.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02131662
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 2
Start date May 15, 2014
Completion date May 4, 2016
View Details
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