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



Status:Terminated
Conditions:Women's Studies, Endometriosis
Therapuetic Areas:Other, Reproductive
Healthy:No
Age Range:18 - 48
Updated:2/14/2019
Start Date:February 28, 2009
End Date:August 31, 2009

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A Randomized, Double-blind Study Evaluating the Safety and Efficacy of Proellex® in the Treatment of Premenopausal Women With Symptomatic Endometriosis-extension Study

ZPE-201 Extension of treatment

This is an extension of the phase II, three-arm, parallel design, dose-ranging,
placebo-controlled, randomized, double-blind, multicenter study in which placebo or one (1)
of two (2) dose levels of Proellex® was administered once-daily for four (4) months.

Inclusion Criteria:

- Only subjects treated in the ZPE-201 study will be allowed to enter the extension
study.

- Subjects who withdrew from ZPE-201 due to lack of treatment efficacy will also be
invited to participate.

Exclusion Criteria:

- All other subjects
We found this trial at
8
sites
San Diego, California 92108
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San Diego, CA
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600 New Waverly Place
Cary, North Carolina 27518
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Cary, NC
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20 West Wenger Road
Miamisburg, Ohio 45322
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Miamisburg, OH
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7940 Floyd Curl Drive
San Antonio, Texas 78229
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San Antonio, TX
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7940 Floyd Curl Drive
San Antonio, Texas 78229
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San Antonio, TX
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San Ramon, California 94583
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San Ramon, CA
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Tucson, Arizona 85712
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Tucson, AZ
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West Palm Beach, Florida 33409
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West Palm Beach, FL
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