134
Participants
Start Date
November 30, 2009
Primary Completion Date
October 31, 2012
Study Completion Date
October 31, 2012
ChemoFX Assay
Test of an algorithm to predict pathologic response in patients treated with neoadjuvant chemotherapy for breast cancer.
Beth Israel Medical Center, New York
Magee Womens Hospital, Pittsburgh
Breast Care Specialists, P.C., Allentown
Virginia Oncology Associates, Norfolk
Advanced Breast Care, Marietta
Advanced Medical Specialties, Miami
Advantage Clinical Research, Nashville
Tennessee Breast Specialists, Nashville
Breast Clinic of Memphis, Germantown
Aurora Sinai Medical Center, Milwaukee
Missouri Cancer Associates, Columbia
OU Medical Center, Oklahoma City
Dallas Surgical Group, Dallas
Leading Edge Research, PA, Dallas
Texas Oncology - Dallas Presbyterian Hospital, Dallas
Texas Oncology - Baylor Charles A. Sammons Cancer Center, Dallas
Texas Oncology - Tyler, Tyler
Texas Oncology - Bedford, Bedford
Southlake Oncology, Southlake
Texas Oncology - Memorial City, Houston
Cancer Care Centers of South Texas, San Antonio
Comprehensive Cancer Centers of Nevada, Henderson
Breast Care, Las Vegas
USC/Norris Comprehensive Cancer Center, Los Angeles
Breastlink Medical Group, Inc, Long Beach
Willamette Valley Cancer Institute and Research Center, Springfield
Morristown Memorial Hospital, Morristown
Women & Infants Hospital, Providence
Lead Sponsor
United States Department of Defense
FED
Precision Therapeutics
INDUSTRY