32 studies found for:    Proellex
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Rank Status Study
1 Completed Study of Proellex in Pre-menopausal Women With Symptomatic Uterine Fibroids
Condition: Uterine Fibroids
Interventions: Drug: 12.5 mg Proellex;   Drug: 25 mg Proellex;   Drug: Placebo
2 Completed Proellex Pharmacokinetics Bridging Study
Condition: Healthy
Interventions: Drug: 25 mg Proellex;   Drug: 50 mg Proellex
3 Completed A Study of Progenta (CDB-4124) in Pre-menopausal Women With Symptomatic Leiomyomata
Condition: Uterine Leiomyomata
Interventions: Drug: Progenta;   Drug: Lucron Depot;   Drug: Placebo
4 Completed
Has Results
Two Year Extension Study of the Selective Progesterone Receptor Modulator Proellex® (CDB-4124) in Pre-Menopausal Women With Symptomatic Leiomyomata Who Have Previously Completed Study ZPU 003
Condition: Uterine Fibroids
Interventions: Drug: Proellex®;   Drug: Placebo
5 Completed Safety, Pharmacokinetics and Efficacy of Proellex® (Telapristone Acetate) Administered Vaginally in the Treatment of Premenopausal Women With Uterine Fibroids Who Have Completed ZPV-200
Condition: Uterine Fibroids
Interventions: Drug: Proellex 12 mg;   Drug: Proellex 24 mg
6 Terminated Evaluating the Safety and Efficacy of Proellex® (CDB-4124) in Premenopausal Women With Symptomatic Uterine Fibroids
Condition: Uterine Fibroids
Interventions: Drug: Proellex®;   Drug: Placebo
7 Completed Proellex® Pharmacokinetic Bridging Study II
Condition: Healthy
Intervention: Drug: Proellex 25 mg
8 Terminated Multicenter Study Evaluating the Safety of Proellex® in Premenopausal Women With Uterine Fibroids
Condition: Uterine Fibroids
Interventions: Drug: Proellex® 25 mg;   Drug: Proellex® 50 mg
9 Completed Evaluate the Safety and PK of Proellex® in Female Patients With Impaired Hepatic Function and Healthy Adults
Conditions: Impaired Liver Function;   Healthy Volunteers
Intervention: Drug: Proellex
10 Completed Investigate Absorption, Metabolism and Excretion of [14C}-Proellex Following Single Oral Dose in Healthy Females
Conditions: ABSORPTION;   METABOLISM;   EXCRETION
Intervention: Drug: Proellex
11 Withdrawn Safety and Efficacy of 25 and 50 mg Doses of Proellex® in Treating the Recurrence of Uterine Fibroid Symptoms
Condition: Uterine Fibroids
Intervention: Drug: Proellex
12 Completed Evaluation of Safety, Pharmacokinetics, and Efficacy of Proellex Administered Vaginally in Women With Uterine Fibroids
Condition: Uterine Fibroids
Intervention: Drug: telapristone acetate
13 Completed A Safety and Pharmacokinetic Study of Proellex®
Condition: Healthy
Intervention: Drug: Proellex
14 Terminated Study to Evaluate Menses Induction in Women Administered Proellex
Condition: Amenorrhea
Interventions: Drug: Placebo;   Drug: Proellex
15 Completed Comparison of Two Formulations of Proellex for Vaginal Administration
Condition: Comparison of 2 Different Formulations of 12 mg Proellex Vaginal Capsules
Interventions: Drug: Proellex Formulation A;   Drug: Proellex Formulation B
16 Recruiting Comparison of Two Formulations of Proellex for Oral Administration
Condition: Healthy
Interventions: Drug: Telapristone Acetate, Proellex 12 mg Formulation A;   Drug: Telapristone Acetate, Proellex 12 mg Formulation B
17 Completed Open-Label, Multiple-Dose, Non-Randomized Study to Assess Drug-Drug Interactions of Proellex® in Female Subjects
Condition: Drug Interactions
Intervention: Drug: Proellex®
18 Terminated Study Evaluating the Safety and Efficacy of Proellex® in the Treatment of Endometriosis-extension Study
Condition: Endometriosis
Intervention: Drug: Proellex®
19 Terminated Pharmacokinetics, Safety and Efficacy Study of Proellex in Pre-menopausal Women With Symptomatic Uterine Fibroids
Condition: Uterine Fibroids
Interventions: Drug: Proellex 25 mg;   Drug: Proellex 50 mg;   Drug: Lupron Depot
20 Terminated Safety of 25 and 50 mg Proellex® in the Treatment of Women With Symptomatic Uterine Fibroids
Condition: Uterine Fibroids
Intervention: Drug: Proellex

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Indicates status has not been verified in more than two years