Found 36 matching trials
A Safety and Pharmacokinetic Study of Proellex® PHASE1 Dose escalating study of 7 daily doses of Proellex at 100 mg, 150 mg and 20...
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Healthcare Discoveries Inc.
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Extension Study of Proellex in Women Who Have Previously Completed Study ZPU 003 PHASE2 ZPU-003 EXT is a 2-year extension study of ZPU-003 (NCT00882258) to determi...
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Women's Health Research
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Safety and Efficacy Study to Evaluate Proellex in the Treatment of Premenopausal Women With Symptomatic Endometriosis PHASE2 The purpose of this study is to determine whether Proellex is safe and effe...
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Advanced Clinical Therapeutics, LLC
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Crossover Study of the Safety and PK Properties of Proellex® PHASE1 Study to evaluate the PK of 25 mg and 50 mg of Proellex from 2 different su...
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Healthcare Discoveries Inc.
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Study of Proellex in Pre-menopausal Women With Symptomatic Uterine Fibroids PHASE2 Two (2) dose levels of Proellex or placebo will be administered once-daily ...
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Alabama Clinical Therapeutics, LLC
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A Multi-Center, Parallel Design, Randomized, Double-Blind Study to Evaluate the Safety and Efficacy of 6 and 12 mg Proellex® (Telapristone Acetate) Administered Orally in the Treatment of Premenopausal Women With Confirmed Symptomatic Uterine Fibroids PHASE2 The primary objective of this study is to determine the safety and efficacy...
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Alabama Clinical Therapeutics, LLC
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Comparison of Two Formulations of Proellex for Vaginal Administration PHASE1 This study is a double-blind crossover study in female healthy volunteers t...
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Multiple Locations
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Safety and Efficacy of Proellex in Pre-menopausal Anemic Women With Symptomatic Uterine Fibroids PHASE3 Eligible female subjects will be randomly assigned to one of the three trea...
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Alabama Clinical Therapeutics
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Safety and Efficacy of Telapristone Acetate (Proellex®) in the Treatment of Pre-Menopausal Women With Confirmed, Symptomatic Endometriosis PHASE2 The primary purpose of this study is to determine the safety and efficacy o...
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Multiple Locations
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Open-Label Extension Study to ZPE-202 PHASE2 This study is a phase 2, open-label extension study of 12 mg Proellex for 2...
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Multiple Locations
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