drugset / Trial / NCT01156857

PGL4001 Efficacy Assessment in Reduction of Symptoms Due to Uterine Leiomyomata

NCT01156857

Phase 3 Completed 209 enrolled PregLem SA
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a multicentre, Phase III, efficacy and safety open-label study with PGL4001 10mg once daily for 3 months, blinded towards the administration of progestin or placebo after end of PGL4001 treatment.

Timeline

Start
2010-07
Primary completion
2011-11
Completion
2012-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Norethindrone Unknown 10 mg Oral
Subject Ulipristal Acetate Unknown 10 mg Oral

Indications