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33 studies found for:    Proellex
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Rank Status Study
1 Completed Proellex Pharmacokinetics Bridging Study
Condition: Healthy
Interventions: Drug: 25 mg Proellex;   Drug: 50 mg Proellex
2 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
3 Completed
Has Results
Evaluate the Safety and PK of Proellex® in Female Patients With Impaired Hepatic Function and Healthy Adults
Condition: Impaired Liver Function
Intervention: Drug: Proellex
4 Terminated
Has Results
Study to Evaluate Menses Induction in Women Administered Proellex
Condition: Amenorrhea
Interventions: Drug: Placebo;   Drug: Proellex
5 Terminated
Has Results
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
6 Terminated
Has Results
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
7 Terminated
Has Results
Evaluating the Safety and Efficacy of Proellex® (CDB-4124) in Premenopausal Women With Symptomatic Uterine Fibroids
Condition: Uterine Fibroids
Interventions: Drug: Proellex;   Drug: Placebo
8 Terminated
Has Results
Evaluate PK and Safety of Proellex® in Females With Various Stages of Impaired Renal Function and Healthy Females
Condition: Renal Impairment
Intervention: Drug: 50 mg Proellex
9 Terminated
Has Results
Safety and Efficacy of Proellex in Pre-Menopausal Anemic Women With Symptomatic Uterine Fibroids
Conditions: Uterine Fibroids;   Anemia
Interventions: Drug: Proellex 25 mg;   Drug: Proellex 50 mg;   Drug: Placebo
10 Completed
Has Results
Evaluation of Safety, Pharmacokinetics, and Efficacy of Proellex Administered Vaginally in Women With Uterine Fibroids
Condition: Uterine Fibroids
Intervention: Drug: Proellex
11 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
12 Completed Proellex® Pharmacokinetic Bridging Study II
Condition: Healthy
Intervention: Drug: Proellex 25 mg
13 Completed Investigate Absorption, Metabolism and Excretion of [14C}-Proellex Following Single Oral Dose in Healthy Females
Conditions: ABSORPTION;   METABOLISM;   EXCRETION
Intervention: Drug: Proellex
14 Terminated
Has Results
Evaluating the Safety and Efficacy of Proellex® in Premenopausal Women With Symptomatic Uterine Fibroids
Condition: Uterine Fibroids
Interventions: Drug: Proellex;   Other: placebo
15 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
16 Completed
Has Results
Extension Study of Proellex in Women Who Have Previously Completed Study ZPU 003
Condition: Uterine Fibroids
Interventions: Drug: Proellex®;   Drug: Placebo
17 Terminated
Has Results
An Extension Study Evaluating Safety and Efficacy of Proellex® In Women Who Have Previously Completed ZPU 003 Ext
Condition: Uterine Fibroids
Intervention: Drug: 25 mg Proellex
18 Completed
Has Results
A Safety and Pharmacokinetic Study of Proellex®
Condition: Healthy
Intervention: Drug: Proellex
19 Terminated Study Evaluating the Safety and Efficacy of Proellex® in the Treatment of Endometriosis-extension Study
Condition: Endometriosis
Intervention: Drug: Proellex®
20 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

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Indicates status has not been verified in more than two years