# PGL4001 Efficacy Assessment in Reduction of Symptoms Due to Uterine Leiomyomata

> **NCT01156857** · PHASE3 · COMPLETED · sponsor: **PregLem SA** · enrollment: 209 (actual)

## Conditions studied

- Uterine Fibroids

## Interventions

- **DRUG:** PGL4001, placebo
- **DRUG:** PGL4001, progestin

## Key facts

- **NCT ID:** NCT01156857
- **Lead sponsor:** PregLem SA
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2010-07
- **Primary completion:** 2011-11
- **Final completion:** 2012-02
- **Target enrollment:** 209 (ACTUAL)
- **Last updated:** 2016-01-15


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01156857

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01156857, "PGL4001 Efficacy Assessment in Reduction of Symptoms Due to Uterine Leiomyomata". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT01156857. Licensed CC0.

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