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📊 Resource Allocation by Research Phase:
📚 Data Analysis
🧪 Experimental Design
🔬 Clinical Trials
💊 Treatment Development
The purpose of this study is to determine whether Proellex is safe and effe...
Status
Terminated
Location
Advanced Clinical Therapeutics, LLC
Start Date
2007-11
Trial ID
NCT00556075
Treatments Being Tested
Study to evaluate the PK of 25 mg and 50 mg of Proellex from 2 different su...
Status
Completed
Location
Healthcare Discoveries Inc.
Start Date
2008-08-11
Trial ID
NCT00749879
Treatments Being Tested
Eligible female subjects will be randomly assigned to one of the three trea...
Status
Terminated
Location
Alabama Clinical Therapeutics
Start Date
2008-06
Trial ID
NCT00702702
Treatments Being Tested
Subjects will be randomly assigned to one of 3 treatment groups and receive...
Status
Terminated
Location
Hospital Perinatal del Estado de Mexico del ISEM
Start Date
2008-10
Trial ID
NCT00785356
Treatments Being Tested
Safety and efficacy study of 25 and 50 mg doses of Proellex...
Status
Terminated
Location
Visions Clinical Research
Start Date
2009-04
Trial ID
NCT01069120
PK and safety profile of Proellex® in females with various stages of impair...
Status
Terminated
Location
Clinical Pharmacology of Miami, Inc
Start Date
2008-10
Trial ID
NCT00787618
Treatments Being Tested
Premenopausal women with symptomatic uterine fibroids will be randomized to...
Status
Terminated
Location
Advanced Clinical Research Institute
Start Date
2009-02
Trial ID
NCT00853567
The safety of Proellex 25 and 50 mg administered once daily for three treat...
Status
Terminated
Location
Lynn Institute of the Ozarks
Start Date
2008-10
Trial ID
NCT00737282
Treatments Being Tested
Healthy female subjects received a single dose of four different types of P...
Status
Completed
Location
Healthcare Discoveries, Inc
Start Date
2007-06
Trial ID
NCT01067807
Treatments Being Tested
Subjects with symptomatic uterine fibroids will be enrolled and will receiv...
Status
Withdrawn
Location
Genesis Center for Clinical Research
Start Date
TBD
Trial ID
NCT00874302