drugset / Trial / NCT01156857
PGL4001 Efficacy Assessment in Reduction of Symptoms Due to Uterine Leiomyomata
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Norethindrone | Unknown | 10 mg | Oral |
| Subject | Ulipristal Acetate | Unknown | 10 mg | Oral |