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Trial Phases

Phase 12
Phase 27
Phase 32
Phase 41

Trial Status

Completed10
Terminated2

Role Distribution

Other Roles12

Activity Timeline

Clinical Trials (12)

NCT01984398Phase 1Completed
Comparison of Two Formulations of Androxal
Bioequivalence
StudydirectorStart date: 2013-12-31

Showing 10 of 12 trials

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CO
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Clinical Trials (12)

Showing 12 of 12 trials

NCT04320745Phase 4StudyDirector

A Study to Evaluate Androderm®'s Effect on Blood Pressure in Adult Hypogonodal Male Participants

Hypogonadism
Completed
NCT02811159Phase 2StudyDirector

An Extension Study of 12 mg Proellex® (Telapristone Acetate) Administered Orally in the Treatment of Premenopausal Women With Confirmed Symptomatic Uterine Fibroids

Uterine Fibroids
Terminated
NCT02651688Phase 2StudyDirector

A Multi-Center Study in Men With Acquired Hypogonadotropic Hypogonadism to Compare Changes in Body Composition and Metabolic Parameters With Diet and Exercise in Conjunction With Treatment With 12.5 mg or 25 mg Enclomiphene

Acquired Hypogonadotropic HypogonadismObesity
Completed
NCT02301897Phase 2StudyDirector

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

Uterine Fibroids
Completed
NCT02323646Phase 2StudyDirector

Safety and Efficacy of Telapristone Acetate (Proellex®) Administered Vaginally for the Treatment of Uterine Fibroids

Uterine Fibroids
Completed
NCT02147197Phase 3StudyDirector

A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas

LeiomyomaUterine Hemorrhage
Completed
NCT02147158Phase 3StudyDirector

A Study of the Efficacy and Safety of Ulipristal Acetate Intermittent Treatment for Abnormal Uterine Bleeding Associated With Leiomyomas

LeiomyomaUterine Hemorrhage
Completed
NCT01984398Phase 1StudyDirector

Comparison of Two Formulations of Androxal

Bioequivalence
Completed
NCT01728454Phase 2StudyDirector

Safety and Efficacy of Telapristone Acetate (Proellex®) in the Treatment of Pre-Menopausal Women With Confirmed, Symptomatic Endometriosis

Endometriosis
Completed
NCT00958412Phase 2StudyDirector

Study Evaluating the Safety and Efficacy of Proellex® in the Treatment of Endometriosis-extension Study

Endometriosis
Terminated
NCT00749879Phase 1StudyDirector

Crossover Study of the Safety and PK Properties of Proellex®

Pharmacokinetics
Completed
NCT00958334Phase 2StudyDirector

Extension Study of Proellex in Women Who Have Previously Completed Study ZPU 003

Uterine Fibroids
Completed

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