Safety and Efficacy Study to Evaluate Proellex in the Treatment of Premenopausal Women With Symptomatic Endometriosis - Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00556075

Locations


United States, Arizona
	Advanced Clinical Therapeutics, LLC
	Tucson, Arizona, United States, 85712

United States, Arkansas
	Lynn Institute of the Ozarks
	Little Rock, Arkansas, United States, 72205

United States, California
	Compass Clinical Research
	San Ramon, California, United States, 94583
	Medical Center for Clinical Research
	San Diego, California, United States, 92108

United States, Florida
	Comprehensive Clinical Trials
	West Palm Beach, Florida, United States, 33409
	Altus Research
	Lake Worth, Florida, United States, 33461

United States, Iowa
	Medical Associates
	Dubuque, Iowa, United States, 52002

United States, North Carolina
	Wake Research Associates
	Raleigh, North Carolina, United States, 27612
	Physicians for Women
	Cary, North Carolina, United States, 27511

United States, Ohio
	HWC Women's Research Center
	Miamisburg, Ohio, United States, 45342
	Rapid Medical Research, Inc.
	Cleveland, Ohio, United States, 44122

United States, South Carolina
	SC Clinical Research Center, LLC
	Columbia, South Carolina, United States, 29201
	Greenville Pharma Research
	Greenville, South Carolina, United States, 29615
	Gaffney Pharmaceutical Research
	Gaffney, South Carolina, United States, 29340

United States, Texas
	Advanced Research Associates
	Corpus Christi, Texas, United States, 78414
	Clinical Trials of Texas/Seven Oaks Women's Center
	San Antonio, Texas, United States, 78229
	Clinical Trials of Texas/Institute for Women's Health
	San Antonio, Texas, United States, 78229

Sponsors and Collaborators

Repros Therapeutics Inc.

Investigators


Study Director:	Andre vanAs, MD, PhD	Repros Therapeutics Inc.