Search
Paclitaxel Treatment Options in Canada
A collection of 344 research studies where Paclitaxel is the interventional treatment. These studies are located in the Canada . Paclitaxel is used for conditions such as Breast Cancer, Ovarian Cancer and Non-Small Cell Lung Cancer.
301 - 312 of 344
Show Filters
Match to Clinical Trials
Access to cutting-edge treatments
Latest clinical trials
Find trials in your area
Search by Name
Filter by Condition
Filter by Age
Filter by Type
Gender
Male
Female
Both
Type of Study
Interventional
Observational
Clinical Trial Phase
Phase 1
Phase 2
Phase 3
Phase 4
Phase 1/2
Phase 2/3
Unknown
A Study of AC Followed by a Combination of Paclitaxel Plus Trastuzumab or Lapatinib or Both Given Before Surgery to Patients With Operable HER2 Positive Invasive Breast Cancer
Unknown
The primary purpose of this study is to determine whether breast cancer tumors respond (as measured by pathologic complete response: the absence of microscopic evidence of invasive tumor cells in the breast) to combined chemotherapy of AC(doxorubicin and cyclophosphamide) followed by paclitaxel plus trastuzumab or lapatinib or both given before surgery to patients with HER2-positive breast cancer. Trastuzumab will also be given to all patients after surgery. The study will also evaluate the toxi... Read More
The primary purpose of this study is to determine whether breast cancer tumors respond (as measured by pathologic complete response: the absence of microscopic evidence of invasive tumor cells in the breast) to combined chemotherapy of AC(doxorubicin and cyclophosphamide) followed by paclitaxel plus trastuzumab or lapatinib or both given before surgery to patients with HER2-positive breast cancer. Trastuzumab will also be given to all patients after surgery. The study will also evaluate the toxic effects of the chemotherapy combination, including effects on the heart, and will determine survival and progression-free survival 5 years after treatment. Also, the study will look at whether there are gene expression profiles in the tumor tissue that can predict pathologic complete response. Read Less
Gender:
FEMALE
Ages:
18 years and above
Trial Updated:
06/03/2016
Locations: MBCCOP, Gulf Coast, Mobile, Alabama +109 locations
MBCCOP, Gulf Coast, Mobile, Alabama
Scripps Cancer Center-San Diego, La Jolla, California
University of California, Irvine Medical Center, Long Beach, California
Pacific Shores Medical Group, Long Beach, California
St. Joseph Hospital, Orange, California
Desert Regional Medical Center Comprehensive Cancer Center, Palm Springs, California
Stanford University Medical Center, Palo Alto, California
Sutter Medical Center, Sacramento, California
Kaiser Permanente-San Diego, San Diego, California
Santa Rosa Memorial Hospital, Santa Rosa, California
Kaiser Permanente-Vallejo, Vallejo, California
University of Colorado Cancer Center, Aurora, Colorado
Memorial Hospital, Colorado Springs, Colorado
Kaiser Permanente-Franklin, Denver, Colorado
CCOP-Colorado Cancer Research Prog. Inc.(Administrative Only), Denver, Colorado
Kaiser Permanente Rock Creek, Lafayette, Colorado
Hartford Hospital, Hartford, Connecticut
Eastern Connecticut Hematology & Oncology Associates, Norwich, Connecticut
Sibley Memorial Hospital, Washington, District of Columbia
MD Anderson Cancer Center, Orlando, Florida
Phoebe Putney Memorial Hospital, Albany, Georgia
MBCCOP, Medical College of Georgia Research Institute, Augusta, Georgia
University of Hawaii, Honolulu, Hawaii
Kaiser Permanente Hawaii - Moanalua Med Center, Honolulu, Hawaii
Kootenai Cancer Center, Coeur D'Alene, Idaho
Rush University Medical Center, Chicago, Illinois
Decatur Memorial Hospital, Decatur, Illinois
Cancer Institute at Alexian Brothers Hospital Network, Elk Grove, Illinois
Edward Hospital, Naperville, Illinois
Edward Cancer Center Plainfield, Plainfield, Illinois
CCOP, Central Illinois, Springfield, Illinois
CCOP, Carle Cancer Center, Urbana, Illinois
St. Vincent Hospital and Health Care Center, Indianapolis, Indiana
CCOP, Northern Indiana Cancer Research Consortium, South Bend, Indiana
CCOP, Des Moines, IA, Des Moines, Iowa
University of Iowa, Iowa City, Iowa
CCOP, Sioux Community Cancer consortium, Sioux City, Iowa
CCOP, Wichita KS, Wichita, Kansas
University of Kentucky Medical Center, Lexington, Kentucky
NortonHealtcare Inc., Louisville, Kentucky
CCOP, Ochsner Clinic Foundation, New Orleans, Louisiana
Greater Baltimore Medical Center, Baltimore, Maryland
Franklin Square Hospital Center, Baltimore, Maryland
Boston Medical Center, Boston, Massachusetts
CCOP, Michigan Cancer Research Consortium, Ann Arbor, Michigan
Henry Ford Health System, Detroit, Michigan
Henry Ford Hospital, Detroit, Michigan
CCOP, Grand Rapids Clnical Oncology Program, Grand Rapids, Michigan
CCOP, Kalamazoo, MI, Kalamazoo, Michigan
Michigan State University - Breslin Cancer Center, Lansing, Michigan
CCOP, William Beaumont Hospital, Royal Oak, Michigan
Providence Hospital - Southfield, Southfield, Michigan
Hennepin County Medical Center, Minneapolis, Minnesota
CCOP, Metro-Minnesota, Minneapolis, Minnesota
University of Missouri-Ellis Fischel, Columbia, Missouri
CCOP, Kansas City (Administrative Only), Kansas City, Missouri
CCOP, Ozark Health Ventures LLC, Springfield, Missouri
Saint Louis UniversityHealth Sciences Center, St. Louis, Missouri
CCOP, Heartland Cancer Research, St. Louis, Missouri
CCOP, Montana Cancer Consortium, Billings, Montana
CCOP, Missouri Valley Consortium, Omaha, Nebraska
Cancer Institute of New Jersey, New Brunswick, New Jersey
Newark Beth Israel Medical Center, Newark, New Jersey
New York Oncology Hematology PC-Albany, Albany, New York
Cancer Center at Glens Falls Hospital, Glens Falls, New York
CCOP, Hematology-Oncology Associates of CNY, Syracuse, New York
Alamance Regional Medical Center, Burlington, North Carolina
University of North Carolina at Chapel Hill, Chapel Hill, North Carolina
CCOP, Southeast Cancer Control Consortium, Charlotte, North Carolina
Alamance Regional Medical Center - Off site Clinic, Mebane, North Carolina
Wake Forest University School of Medicine, Winston-Salem, North Carolina
Akron City Hospital, Akron, Ohio
Aultman Hospital, Canton, Ohio
Case Western Reserve/University Hospitals-Ireland Cancer Cntr., Cleveland, Ohio
Ohio State University, Columbus, Ohio
CCOP, Columbus, OH, Columbus, Ohio
CCOP, Dayton, OH, Dayton, Ohio
CCOP, Oklahoma, Tulsa, Oklahoma
Lehigh Valley Hospital, Allentown, Pennsylvania
Geisinger Clinic, Danville, Pennsylvania
Hershey Medical Center, Hershey, Pennsylvania
Albert Einstein Healthcare Network, Philadelphia, Pennsylvania
Allegheny General Hospital/Allegheny-Singer Research Institute, Pittsburgh, Pennsylvania
NSABP Foundation, Inc., Pittsburgh, Pennsylvania
University of Pittsburgh, Pittsburgh, Pennsylvania
Western Pennsylvania Hospital, Pittsburgh, Pennsylvania
Mercy Hospital, Scranton, Pennsylvania
Reading Hospital & Medical Center, West Reading, Pennsylvania
CCOP, Main Line Health, Wynnewood, Pennsylvania
CCOP, Upstate Carolina, Spartanburg, South Carolina
Sanford Cancer Center, Souix Falls, South Dakota
Thompson Cancer Survival Center-Dowell Springs, Knoxville, Tennessee
Joe Arrington Cancer Research & Treatment Center, Lubbock, Texas
University of Texas Health Science Center at San Antonio, San Antonio, Texas
MBCCOP, Virginia Commonwealth University, Richmond, Virginia
Puget Sound Oncology Consortium, Seattle, Washington
CCOP, Virginia Mason, Seattle, Washington
CCOP, Northwest, Tacoma, Washington
West Virginia University Hospitals Inc., Morgantown, West Virginia
Camden-Clark Memorial Hospital, Parkersburg, West Virginia
Wheeling Hospital, Wheeling, West Virginia
CCOP, Marshfield Clinic, Marshfield, Wisconsin
Medical College of Wisconsin, Milwaukee, Wisconsin
Odette Cancer Centre, Toronto, Ontario
Royal Victoria Hospital, Montreal, Quebec
Jewish General Hospital, Montreal, Quebec
St. Mary's Hospital Center, Montreal, Quebec
University of Montreal Hospital Group, Montreal, Quebec
Centre Hospitalier Affilie Universitaire De Quebec, Hospital du St-Sacrement, Quebec City, Quebec
MBCCOP, San Juan, Puerto Rico, San Juan, Not set
Conditions: Invasive Breast Cancer
Chemotherapy and Radiation in Treating Participants With Stage 3 Non-Small Cell Lung Cancer
Completed
This study will compare the overall survival of participants with locally-advanced, Stage III Non-Small Cell Lung Cancer (NSCLC) with nonsquamous cell histology.
This study will compare the overall survival of participants with locally-advanced, Stage III Non-Small Cell Lung Cancer (NSCLC) with nonsquamous cell histology. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
05/20/2016
Locations: For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Birmingham, Alabama +132 locations
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Birmingham, Alabama
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Scottsdale, Arizona
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Tucson, Arizona
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Fayetteville, Arkansas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Duarte, California
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Fountain Valley, California
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., La Jolla, California
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., New Haven, Connecticut
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Hollywood, Florida
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Tampa, Florida
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., West Palm Beach, Florida
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Athens, Georgia
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Marietta, Georgia
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Thomasville, Georgia
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Chicago, Illinois
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Quincy, Illinois
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Evansville, Indiana
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Indianapolis, Indiana
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., New Albany, Indiana
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Westwood, Kansas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Wichita, Kansas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Louisville, Kentucky
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Columbia, Maryland
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Fairhaven, Massachusetts
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Ann Arbor, Michigan
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Minneapolis, Minnesota
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Kansas City, Missouri
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., St Louis, Missouri
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Bronx, New York
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., New York, New York
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Fargo, North Dakota
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Cincinnati, Ohio
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Charleston, South Carolina
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Chattanooga, Tennessee
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Memphis, Tennessee
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Nashville, Tennessee
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Bedford, Texas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Dallas, Texas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Longview, Texas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Odessa, Texas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., San Marcos, Texas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Sherman, Texas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Sugar Land, Texas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., The Woodlands, Texas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Wichita Falls, Texas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Burlington, Vermont
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Spokane, Washington
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Vancouver, Washington
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Morgantown, West Virginia
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Madison, Wisconsin
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Buenos Aires, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Wollongong, New South Wales
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Launceston, Tasmania
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Frankston, Victoria
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Antwerp, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Edegem, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Gent, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Gilly, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Haine-St.- Paul, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Leuven, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Namur, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Turnhout, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Barretos, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Curitiba, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Porto Alegre, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Rio De Janeiro, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., São Paulo, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Edmonton, Alberta
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., London, Ontario
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Newmarket, Ontario
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Toronto, Ontario
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Montreal, Quebec
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Beijing, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Guang Zhou, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Jinan, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Shanghai, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Sichuan, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Wu Han, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Bayonne, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Lille, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Paris, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Pierre Benite, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Erlangen, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Frankfurt, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Hannover, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Hemer, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Immenhausen, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Köln, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Mainz, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Mannheim, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Oldenburg, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Rheine, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Ulm, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Athens, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Patras, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Bangalore, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Hyderabaad, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Jaipur, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Kolkata, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Madurai, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Mumbai, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Trivandrum, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Dublin, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Incheon, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Seoul, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Suwon-City, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Amsterdam, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Breda, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., S-Hertogenbosch, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Lisbon, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Santa Maria Da Feira, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Vila Franca De Xira, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Alicante, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Badalona, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Elche, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Hospitalet De Llobregat, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Madrid, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Majadahonda, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Pamplona, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Terrassa, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Kaohsiung, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Kuei Shan Hsiang, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Taichung, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Taipei, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Fatih, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Gaziantep, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Izmir, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Melikgazi, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Umuttepe, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Edgbaston, Birmingham
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., London, Greater London
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Edinburgh, Scotland
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Manchester, Not set
Conditions: Non Small Cell Lung Cancer
A Study of the Addition of Avastin (Bevacizumab) to Carboplatin and Paclitaxel Therapy in Patients With Ovarian Cancer
Completed
This open-label, non-comparative, multi-center study will assess the safety profile and efficacy of Avastin (bevacizumab) when added to carboplatin and paclitaxel therapy in participants with epithelial ovarian cancer, fallopian tube carcinoma or primary peritoneal carcinoma. Participants will receive 15 milligrams/kilogram (mg/kg) Avastin intravenously (IV) on Day 1 of every cycle for up to 36 cycles of 3 weeks each, carboplatin (area under the plasma concentration-time curve \[AUC\] 5-6 mg/ml/... Read More
This open-label, non-comparative, multi-center study will assess the safety profile and efficacy of Avastin (bevacizumab) when added to carboplatin and paclitaxel therapy in participants with epithelial ovarian cancer, fallopian tube carcinoma or primary peritoneal carcinoma. Participants will receive 15 milligrams/kilogram (mg/kg) Avastin intravenously (IV) on Day 1 of every cycle for up to 36 cycles of 3 weeks each, carboplatin (area under the plasma concentration-time curve \[AUC\] 5-6 mg/ml/min) on Day 1 every 3 weeks for a maximum of 8 cycles and paclitaxel 175 milligram per square meter (mg/m\^2) on Day 1 every 3 weeks or 80 mg/m\^2 every week for a maximum of 8 cycles. The anticipated time on study drug will be 108 weeks or until disease progression or unacceptable toxicity. Read Less
Gender:
FEMALE
Ages:
18 years and above
Trial Updated:
05/03/2016
Locations: Not set, Buenos Aires, Not set +241 locations
Not set, Buenos Aires, Not set
Not set, Buenos Aires, Not set
Not set, Buenos Aires, Not set
Not set, Rosario, Not set
Not set, Tucuman, Not set
Not set, Graz, Not set
Not set, Graz, Not set
Not set, Innsbruck, Not set
Not set, Ried-innkreis, Not set
Not set, Salzburg, Not set
Not set, Steyr, Not set
Not set, Villach, Not set
Not set, Wien, Not set
Not set, Wien, Not set
Not set, Salvador, BA
Not set, Fortaleza, CE
Not set, Goiania, GO
Not set, Curitiba, PR
Not set, Rio de Janeiro, RJ
Not set, Porto Alegre, RS
Not set, Porto Alegre, RS
Not set, Piracicaba, SP
Not set, Sao Paulo, SP
Not set, Sao Paulo, SP
Not set, Sao Paulo, SP
Not set, Sao Paulo, SP
Not set, Sofia, Not set
Not set, Varna, Not set
Not set, Veliko Tarnovo, Not set
Not set, Calgary, Alberta
Not set, Ottawa, Ontario
Not set, Toronto, Ontario
Not set, Montreal, Quebec
Not set, Quebec, Not set
Not set, Aalborg, Not set
Not set, Roskilde, Not set
Not set, Vejle, Not set
Not set, Cairo, Not set
Not set, Tanta, Not set
Not set, Tallinn, Not set
Not set, Tallinn, Not set
Not set, Tartu, Not set
Not set, Amiens, Not set
Not set, Bordeaux, Not set
Not set, Brest, Not set
Not set, Caen, Not set
Not set, Clermont Ferrand, Not set
Not set, Grenoble, Not set
Not set, Lille, Not set
Not set, Lyon, Not set
Not set, Marseille, Not set
Not set, Mougins, Not set
Not set, Paris, Not set
Not set, Paris, Not set
Not set, Paris, Not set
Not set, Paris, Not set
Not set, Paris, Not set
Not set, Paris, Not set
Not set, Reims CEDEX, Not set
Not set, Strasbourg, Not set
Not set, Toulouse, Not set
Not set, Villejuif, Not set
Not set, Athens, Not set
Not set, Athens, Not set
Not set, Athens, Not set
Not set, Heraklion, Crete, Not set
Not set, Larissa, Not set
Not set, Patras, Not set
Not set, Thessaloniki, Not set
Not set, Hong Kong, Not set
Not set, Hong Kong, Not set
Not set, Budapest, Not set
Not set, Budapest, Not set
Not set, Debrecen, Not set
Not set, Pecs, Not set
Not set, Szeged, Not set
Not set, Bangalore, Not set
Not set, Bangalore, Not set
Not set, Hyderabad, Not set
Not set, Jaipur, Not set
Not set, Kochi, Not set
Not set, New Delhi, Not set
Not set, Pune, Not set
Not set, Dublin, Not set
Not set, Afula, Not set
Not set, Beer Sheva, Not set
Not set, Haifa, Not set
Not set, Haifa, Not set
Not set, Holon, Not set
Not set, Jerusalem, Not set
Not set, Jerusalem, Not set
Not set, Kfar Saba, Not set
Not set, Petach Tikva, Not set
Not set, Ramat Gan, Not set
Not set, Rehovot, Not set
Not set, Tel Aviv, Not set
Not set, Napoli, Campania
Not set, Bologna, Emilia-Romagna
Not set, Meldola, Emilia-Romagna
Not set, Roma, Lazio
Not set, Roma, Lazio
Not set, Genova, Liguria
Not set, Brescia, Lombardia
Not set, Milano, Lombardia
Not set, Milano, Lombardia
Not set, Monza, Lombardia
Not set, Saronno, Lombardia
Not set, Novara, Piemonte
Not set, Torino, Piemonte
Not set, Torino, Piemonte
Not set, Palermo, Sicilia
Not set, Firenze, Toscana
Not set, Pisa, Toscana
Not set, Perugia, Umbria
Not set, Terni, Umbria
Not set, Shuwaikh, Not set
Not set, Daugavpils, Not set
Not set, Riga, Not set
Not set, Riga, Not set
Not set, Kaunas, Not set
Not set, Klaipeda, Not set
Not set, Vilnius, Not set
Not set, Bitola, Not set
Not set, Skopje, Not set
Not set, Distrito Federal, Not set
Not set, Oaxaca, Not set
Not set, Toluca, Not set
Not set, Alkmaar, Not set
Not set, Amsterdam, Not set
Not set, Apeldoorn, Not set
Not set, Blaricum, Not set
Not set, Breda, Not set
Not set, Capelle a/d IJssel, Not set
Not set, Den Haag, Not set
Not set, Den Haag, Not set
Not set, Deventer, Not set
Not set, Dordrecht, Not set
Not set, Eindhoven, Not set
Not set, Leidschendam, Not set
Not set, Rotterdam, Not set
Not set, Sittard-Geleen, Not set
Not set, Utrecht, Not set
Not set, Bydgoszcz, Not set
Not set, Warszawa, Not set
Not set, Porto, Not set
Not set, Bucuresti, Not set
Not set, Cluj Napoca, Not set
Not set, Iasi, Not set
Not set, Barnaul, Not set
Not set, Moscow, Not set
Not set, Obninsk, Kaluzhskaya Region, Not set
Not set, Saint-Petersburg, Not set
Not set, Stavropol, Not set
Not set, UFA, Not set
Not set, Dammam, Not set
Not set, Belgrade, Not set
Not set, Nis, Not set
Not set, Bratislava, Not set
Not set, Kosice, Not set
Not set, Ljubljana, Not set
Not set, Maribor, Not set
Not set, Durban, Not set
Not set, Johannesburg, Not set
Not set, Sandton, Not set
Not set, Elda, Alicante
Not set, Oviedo, Asturias
Not set, Llerena (Badajoz), Badajoz
Not set, Manresa, Barcelona
Not set, Cádiz, Cadiz
Not set, Jerez de La Frontera, Cadiz
Not set, San Sebastian de Los Reyes, Guipuzcoa
Not set, San Sebastian, Guipuzcoa
Not set, Palma De Mallorca, Islas Baleares
Not set, Palma de Mallorca, Islas Baleares
Not set, Santiago de Compostela, La Coruña
Not set, Las Palmas de Gran Canaria, Las Palmas
Not set, Leganes, Madrid
Not set, Reus, Tarragona
Not set, La Laguna, Tenerife
Not set, Santa Cruz de Tenerife, Tenerife
Not set, San Juan, Valencia
Not set, Barakaldo, Vizcaya
Not set, Bilbao, Vizcaya
Not set, Albacete, Not set
Not set, Alicante, Not set
Not set, Badajoz, Not set
Not set, Barcelona, Not set
Not set, Barcelona, Not set
Not set, Barcelona, Not set
Not set, Barcelona, Not set
Not set, Burgos, Not set
Not set, Caceres, Not set
Not set, Castellon, Not set
Not set, Ciudad Real, Not set
Not set, Cordoba, Not set
Not set, Girona, Not set
Not set, Granada, Not set
Not set, Guadalajara, Not set
Not set, Jaen, Not set
Not set, La Coruña, Not set
Not set, Lugo, Not set
Not set, Madrid, Not set
Not set, Madrid, Not set
Not set, Madrid, Not set
Not set, Madrid, Not set
Not set, Madrid, Not set
Not set, Madrid, Not set
Not set, Madrid, Not set
Not set, Malaga, Not set
Not set, Malaga, Not set
Not set, Navarra, Not set
Not set, Salamanca, Not set
Not set, Segovia, Not set
Not set, Sevilla, Not set
Not set, Sevilla, Not set
Not set, Toledo, Not set
Not set, Valencia, Not set
Not set, Valencia, Not set
Not set, Valencia, Not set
Not set, Valencia, Not set
Not set, Valladolid, Not set
Not set, Zaragoza, Not set
Not set, Eskilstuna, Not set
Not set, Falun, Not set
Not set, Karlstad, Not set
Not set, Umeå, Not set
Not set, Uppsala, Not set
Not set, Örebro, Not set
Not set, Aarau, Not set
Not set, Baden, Not set
Not set, Bellinzona, Not set
Not set, Bern, Not set
Not set, Genève 14, Not set
Not set, Zürich, Not set
Not set, Taipei City, Not set
Not set, Taipei City, Not set
Not set, Taoyuan Hsien, Not set
Not set, Ankara, Not set
Not set, Ankara, Not set
Not set, Diyarbakir, Not set
Not set, Istanbul, Not set
Not set, Montevideo, Not set
Conditions: Ovarian Cancer
Phase I/II AZD8931/Paclitaxel in Treatment of Advanced Solid Tumours (Phase I) and Advanced Breast Cancer (Phase II)
Completed
The main purpose of this study is to determine if AZD8931 can improve the efficacy of standard chemotherapy for the treatment of advanced breast cancer. This study will be conducted in 2 parts: the first part (phase I) will determine a dose of AZD8931 that can be safely administered with paclitaxel chemotherapy. The second part (phase II) will determine the efficacy and safety of AZD8931 in combination with paclitaxel chemotherapy in breast cancer.
The main purpose of this study is to determine if AZD8931 can improve the efficacy of standard chemotherapy for the treatment of advanced breast cancer. This study will be conducted in 2 parts: the first part (phase I) will determine a dose of AZD8931 that can be safely administered with paclitaxel chemotherapy. The second part (phase II) will determine the efficacy and safety of AZD8931 in combination with paclitaxel chemotherapy in breast cancer. Read Less
Gender:
ALL
Ages:
Between 18 years and 150 years
Trial Updated:
01/15/2016
Locations: Research Site, Brussels (Jette), Not set +39 locations
Research Site, Brussels (Jette), Not set
Research Site, Leuven, Not set
Research Site, Namur, Not set
Research Site, Sint-Niklaas, Not set
Research Site, Sao Paulo, Not set
Research Site, São Paulo, Not set
Research Site, Sofia, Not set
Research Site, Stara Zagora, Not set
Research Site, Varna, Not set
Research Site, Vratza, Not set
Research Site, Halifax, Nova Scotia
Research Site, London, Ontario
Research Site, Ottawa, Ontario
Research Site, Brno, Not set
Research Site, Jicin, Not set
Research Site, Olomouc, Not set
Research Site, Praha 2, Not set
Research Site, Praha 4 - Krc, Not set
Research Site, Praha 4, Not set
Research Site, Znojmo, Not set
Research Site, Villejuif Cedex, Not set
Research Site, Budapest, Not set
Research Site, Debrecen, Not set
Research Site, Györ, Not set
Research Site, Szeged, Not set
Research Site, Lido di Camaiore, Not set
Research Site, Modena, Not set
Research Site, Treviglio, Not set
Research Site, Ciudad de Panama, Not set
Research Site, Lima, Not set
Research Site, Barcelona, Not set
Research Site, Madrid, Not set
Research Site, Valencia, Not set
Research Site, Uppsala, Not set
Research Site, Chur, Not set
Research Site, Glasgow, Not set
Research Site, Leicester, Not set
Research Site, London, Not set
Research Site, Nottingham, Not set
Research Site, Surrey, Not set
Imetelstat in Combination With Paclitaxel (With or Without Bevacizumab) in Patients With Locally Recurrent or Metastatic Breast Cancer
Completed
The purpose of this study is to evaluate the efficacy and safety of treatment with imetelstat + paclitaxel (with or without bevacizumab) versus paclitaxel (with or without bevacizumab) alone for patients with locally recurrent or metastatic breast cancer who have not received chemotherapy or have received one non-taxane based chemotherapy for metastatic breast cancer.
The purpose of this study is to evaluate the efficacy and safety of treatment with imetelstat + paclitaxel (with or without bevacizumab) versus paclitaxel (with or without bevacizumab) alone for patients with locally recurrent or metastatic breast cancer who have not received chemotherapy or have received one non-taxane based chemotherapy for metastatic breast cancer. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
12/22/2015
Locations: Clearview Cancer Center, Huntsville, Alabama +54 locations
Clearview Cancer Center, Huntsville, Alabama
Alta Bates Summit Medical Center, Berkeley, California
Southbay Oncology Hematology Partners, Campbell, California
Cancer Care Associates, Fresno, California
Memorial Miller Hospital, Long Beach, California
St. Joseph Hospital, Orange, California
Desert Regional Comprehensive Cancer Center, Palm Springs, California
UC San Diego, San Diego, California
Redwood Regional Medical Group, Santa Rosa, California
Univ. Colorado at Denver, Aurora, Colorado
Connecticut Oncology & Hematology, Torrington, Connecticut
Medical Oncology Hematology, Waterbury, Connecticut
Florida Oncology Associates, Jacksonville, Florida
Hematology Oncology Associates, Port St. Lucie, Florida
H. Lee Moffitt Cancer Center, Tampa, Florida
Northeast Georgia Cancer Care, Athens, Georgia
Peachtree Hematology Oncology, Atlanta, Georgia
Emory University, Atlanta, Georgia
Northeast Georgia Medical Center, Gainesville, Georgia
Central Georgia Cancer Care, Macon, Georgia
Summit Cancer Care, Savannah, Georgia
Kootenai Medical Center, Post Falls, Idaho
Ingalls Memorial Hospital, Chicago, Illinois
Rush University, Chicago, Illinois
Mid Illinois Hematology & Oncology, Normal, Illinois
Cancer Treatment Centers of America, Zion, Illinois
Indiana University, Indianapolis, Indiana
Community Hospitals of Indiana, Indianapolis, Indiana
Horizon Oncology Center, Lafayette, Indiana
Cancer Center of Kansas, Wichita, Kansas
Montgomery Cancer Care, Mount Sterling, Kentucky
Michigan State University, East Lansing, Michigan
New Mexico Cancer Center, Albuquerque, New Mexico
Prohealth Associates, Lake Success, New York
Stony Brook University, Stony Brook, New York
Carolinas Hematology/Oncology, Charlotte, North Carolina
Moses Cone Medical System, Greensboro, North Carolina
Case Western Reserve Univ., Cleveland, Ohio
Mercy Physicians of Oklahoma, Oklahoma City, Oklahoma
Cancer Care Associates, Tulsa, Oklahoma
Kaiser Northwest, Portland, Oregon
Pinnacle Health, Harrisburg, Pennsylvania
Penn. State Univ., Hershey, Pennsylvania
The Jones Clinic, Germantown, Tennessee
The West Clinic, Memphis, Tennessee
Scott & White Healthcare, Temple, Texas
Northern Utah Associates, Ogden, Utah
Peninsula Cancer Institute, Newport News, Virginia
Medical Oncology Associates, Spokane, Washington
Northwest Medical Specialties, Tacoma, Washington
Grand River Regional Cancer Centre, Kitchener, Ontario
Stronach Regional Cancer Centre at Southlake, Newmarket, Ontario
The Ottawa Hospital Cancer Centre, Ottawa, Ontario
Sunnybrook Health Services Centre, Toronto, Ontario
McGill University, Montreal, Quebec
Conditions: Locally Recurrent or Metastatic Breast Cancer
Paclitaxel, Cisplatin, and Filgrastim Combined With Radiation Therapy in Treating Patients With Locally Recurrent Head and Neck Cancer
Completed
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Colony-stimulating factors such as filgrastim may increase the number of immune cells found in bone marrow or peripheral blood and may help a person's immune system recover from the side effects of chemotherapy. Radiation therapy uses high-energy x-rays to damage tumor cells.
PURPOSE: Phase II trial to study the effectiveness of paclitaxel, cisplatin, and filgrastim combined w... Read More
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Colony-stimulating factors such as filgrastim may increase the number of immune cells found in bone marrow or peripheral blood and may help a person's immune system recover from the side effects of chemotherapy. Radiation therapy uses high-energy x-rays to damage tumor cells.
PURPOSE: Phase II trial to study the effectiveness of paclitaxel, cisplatin, and filgrastim combined with radiation therapy in treating patients who have locally recurrent head and neck cancer and have received previous treatment with radiation therapy. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
11/14/2015
Locations: University of Alabama at Birmingham Comprehensive Cancer Center, Birmingham, Alabama +234 locations
University of Alabama at Birmingham Comprehensive Cancer Center, Birmingham, Alabama
Comprehensive Cancer Institute of Huntsville, Huntsville, Alabama
Huntsville Hospital System, Huntsville, Alabama
MBCCOP - Gulf Coast, Mobile, Alabama
Alabama Oncology, LLC, Montgomery, Alabama
DCH Cancer Treatment Center, Tuscaloosa, Alabama
Foundation for Cancer Research and Education, Phoenix, Arizona
Mount Diablo Medical Center, Concord, California
City of Hope Comprehensive Cancer Center, Duarte, California
Saint Agnes Cancer Center, Fresno, California
California Cancer Center, Fresno, California
Sutter Health West Cancer Research Group, Greenbrae, California
Loma Linda University Medical Center, Loma Linda, California
Veterans Affairs Medical Center - Long Beach, Long Beach, California
Jonsson Comprehensive Cancer Center, UCLA, Los Angeles, California
USC/Norris Comprehensive Cancer Center and Hospital, Los Angeles, California
CCOP - Bay Area Tumor Institute, Oakland, California
Huntington Cancer Center, Pasadena, California
Robert and Beverly Lewis Family Cancer Care Center, Pomona, California
Radiation Oncology Center - Sacramento, Sacramento, California
Radiation Medical Group, Inc., San Diego, California
UCSF Comprehensive Cancer Center, San Francisco, California
O'Connor Hospital, San Jose, California
CCOP - Santa Rosa Memorial Hospital, Santa Rosa, California
David Grant Medical Center, Travis Air Force Base, California
Memorial Hospital Cancer Center, Colorado Springs, Colorado
University of Colorado Cancer Center, Denver, Colorado
Saint Mary's Hospital and Medical Center, Grand Junction, Colorado
Hospital of St. Raphael, New Haven, Connecticut
CCOP - Christiana Care Health Services, Wilmington, Delaware
University of Florida Health Science Center, Gainesville, Florida
Florida Radiation Oncology Group, Jacksonville, Florida
Health First Holmes Regional Medical Center, Melbourne, Florida
CCOP - Mount Sinai Medical Center, Miami Beach, Florida
Veterans Affairs Medical Center - Miami, Miami, Florida
Sylvester Cancer Center, University of Miami, Miami, Florida
Baptist Hospital of Miami, Miami, Florida
MD Anderson Cancer Center Orlando, Orlando, Florida
Bay Medical Center, Panama City, Florida
Gulf Coast Cancer Treatment Center, Panama City, Florida
Sarasota Radiation and Medical Oncology Center, Sarasota, Florida
Tallahassee Memorial Healthcare, Tallahassee, Florida
H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida
Emory University Hospital - Atlanta, Atlanta, Georgia
CCOP - Atlanta Regional, Atlanta, Georgia
Medical Center/John B. Amos Community Cancer Center, Columbus, Georgia
Regional Radiation Oncology Center at Rome, Rome, Georgia
MBCCOP - Hawaii, Honolulu, Hawaii
Northwest Community Hospital, Arlington Heights, Illinois
Northwestern Memorial Hospital, Chicago, Illinois
CCOP - Central Illinois, Decatur, Illinois
Ingalls Memorial Hospital, Harvey, Illinois
Loyola University Medical Center, Maywood, Illinois
Lutheran General Cancer Care Center, Park Ridge, Illinois
Methodist Medical Center of Illinois, Peoria, Illinois
St. John's Medical Center, Anderson, Indiana
Bloomington Hospital, Bloomington, Indiana
Veterans Affairs Medical Center - Indianapolis (Roudebush), Indianapolis, Indiana
Clarian Health Partners Inc., Indianapolis, Indiana
Regional Cancer Center, Indianapolis, Indiana
Ball Memorial Hospital, Muncie, Indiana
CCOP - Northern Indiana CR Consortium, South Bend, Indiana
Wendt Regional Cancer Center of Finley Hospital, Dubuque, Iowa
Central Baptist Hospital, Lexington, Kentucky
Albert B. Chandler Medical Center, University of Kentucky, Lexington, Kentucky
James Graham Brown Cancer Center, Louisville, Kentucky
Louisville Radiation Oncology, Louisville, Kentucky
Merle M. Mahr Cancer Center, Madisonville, Kentucky
Mary Bird Perkins Cancer Center, Baton Rouge, Louisiana
Tulane University School of Medicine, New Orleans, Louisiana
MBCCOP - LSU Medical Center, New Orleans, Louisiana
CCOP - Ochsner, New Orleans, Louisiana
Maine Medical Center, Portland, Maine
Anne Arundel Oncology Center, Annapolis, Maryland
Marlene and Stewart Greenebaum Cancer Center, University of Maryland, Baltimore, Maryland
Greater Baltimore Medical Center and Cancer Center, Baltimore, Maryland
Harbor Hospital Center, Baltimore, Maryland
Sinai Hospital of Baltimore, Baltimore, Maryland
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland
Peninsula Regional Medical Center, Salisbury, Maryland
Dana-Farber Cancer Institute, Boston, Massachusetts
Cape Cod Hospital, Hyannis, Massachusetts
Veterans Affairs Medical Center - Boston (Jamaica Plain), Jamaica Plain, Massachusetts
CCOP - Ann Arbor Regional, Ann Arbor, Michigan
University of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan
Barbara Ann Karmanos Cancer Institute, Detroit, Michigan
Henry Ford Hospital, Detroit, Michigan
Hurley Medical Center, Flint, Michigan
McLaren Regional Cancer Center, Flint, Michigan
CCOP - Kalamazoo, Kalamazoo, Michigan
Marquette General Hospital, Marquette, Michigan
MidMichigan Medical Center - Midland, Midland, Michigan
CCOP - Beaumont, Royal Oak, Michigan
William Beaumont Hospital, Royal Oak, Michigan
William Beaumont Hospital - Troy, Troy, Michigan
Mayo Clinic Cancer Center, Rochester, Minnesota
CCOP - Metro-Minnesota, Saint Louis Park, Minnesota
Ellis Fischel Cancer Center - Columbia, Columbia, Missouri
CCOP - Kansas City, Kansas City, Missouri
Mallinckrodt Institute of Radiology, Saint Louis, Missouri
St. Louis University Health Sciences Center, Saint Louis, Missouri
Cancer Research for the Ozarks, Springfield, Missouri
CCOP - Cancer Research for the Ozarks, Springfield, Missouri
CCOP - Montana Cancer Consortium, Billings, Montana
CCOP - Missouri Valley Cancer Consortium, Omaha, Nebraska
Methodist Hospital Cancer Center - Omaha, Omaha, Nebraska
Nebraska Health System, Omaha, Nebraska
CCOP - Southern Nevada Cancer Research Foundation, Las Vegas, Nevada
Norris Cotton Cancer Center, Lebanon, New Hampshire
Elliot Regional Cancer Center, Manchester, New Hampshire
Veterans Affairs Medical Center - East Orange, East Orange, New Jersey
John F. Kennedy Medical Center, Edison, New Jersey
Trinitas Hospital - Jersey Street Campus, Elizabeth, New Jersey
Monmouth Medical Center, Long Branch, New Jersey
South Jersey Regional Cancer Center, Millville, New Jersey
Fox Chase Virtua Health Cancer Program at Virtua Memorial Hospital, Mount Holly, New Jersey
Cancer Institute of New Jersey, New Brunswick, New Jersey
Newark Beth Israel Medical Center, Newark, New Jersey
Atlantic City Medical Center, Pomona, New Jersey
Valley Hospital, Ridgewood, New Jersey
Community Medical Center, Toms River, New Jersey
St. Francis Medical Center, Trenton, New Jersey
Associated Radiologists, P.A., Warren, New Jersey
Radiation Oncology Associates of Albuquerque, Albuquerque, New Mexico
Cancer Center of Albany Medical Center, Albany, New York
State University of New York Health Science Center at Brooklyn, Brooklyn, New York
New York Methodist Hospital, Brooklyn, New York
Roswell Park Cancer Institute, Buffalo, New York
Finger Lakes Radiation Oncology Center, Clifton Springs, New York
CCOP - North Shore University Hospital, Manhasset, New York
Herbert Irving Comprehensive Cancer Center, New York, New York
Champlain Valley Physicians Hospital Medical Center, Plattsburgh, New York
Vassar Brothers Medical Center, Poughkeepsie, New York
James P. Wilmot Cancer Center, Rochester, New York
CCOP - Syracuse Hematology-Oncology Associates of Central New York, P.C., Syracuse, New York
Riverhill Radiation Oncology, Yonkers, New York
Lineberger Comprehensive Cancer Center, UNC, Chapel Hill, North Carolina
Northeast Medical Center, Concord, North Carolina
East Carolina University School of Medicine, Greenville, North Carolina
CCOP - Southeast Cancer Control Consortium, Winston-Salem, North Carolina
Comprehensive Cancer Center at Wake Forest University, Winston-Salem, North Carolina
Trinity Cancer Care Center, Minot, North Dakota
Akron General Medical Center, Akron, Ohio
Akron City Hospital, Akron, Ohio
Christ Hospital, Cincinnati, Ohio
Barrett Cancer Center, Cincinnati, Ohio
Ireland Cancer Center, Cleveland, Ohio
University Hospitals of Cleveland, Cleveland, Ohio
Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio
CCOP - Columbus, Columbus, Ohio
Arthur G. James Cancer Hospital - Ohio State University, Columbus, Ohio
CCOP - Dayton, Dayton, Ohio
CCOP - Toledo Community Hospital, Toledo, Ohio
St. Anthony Hospital, Oklahoma City, Oklahoma
University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma
St. John Health System, Tulsa, Oklahoma
CCOP - Oklahoma, Tulsa, Oklahoma
CCOP - Columbia River Program, Portland, Oregon
Lehigh Valley Hospital, Allentown, Pennsylvania
St. Luke's Hospital Cancer Center, Bethlehem, Pennsylvania
Geisinger Medical Center, Danville, Pennsylvania
Mercy Fitzgerald Hospital, Darby, Pennsylvania
Delaware County Memorial Hospital, Drexel Hill, Pennsylvania
Pocono Cancer Center, East Stroudsburg, Pennsylvania
Milton S. Hershey Medical Center, Hershey, Pennsylvania
University of Pennsylvania Cancer Center, Philadelphia, Pennsylvania
Veterans Affairs Medical Center - Philadelphia, Philadelphia, Pennsylvania
Kimmel Cancer Center of Thomas Jefferson University - Philadelphia, Philadelphia, Pennsylvania
Fox Chase Cancer Center, Philadelphia, Pennsylvania
Albert Einstein Cancer Center, Philadelphia, Pennsylvania
University of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania
Mercy Hospital of Pittsburgh, Pittsburgh, Pennsylvania
Western Pennsylvania Hospital, Pittsburgh, Pennsylvania
Reading Hospital and Medical Center, Reading, Pennsylvania
Mercy Hospital Cancer Center - Scranton, Scranton, Pennsylvania
Wilkes Barre General Hospital, Wilkes-Barre, Pennsylvania
York Cancer Center, York, Pennsylvania
Roger Williams Medical Center/BUSM, Providence, Rhode Island
CCOP - Greenville, Greenville, South Carolina
CCOP - Upstate Carolina, Spartanburg, South Carolina
Rapid City Regional Hospital, Rapid City, South Dakota
Jackson-Madison County General Hospital, Jackson, Tennessee
University of Tennessee Cancer Institute, Memphis, Tennessee
Vanderbilt-Ingram Cancer Center, Nashville, Tennessee
Harrington Cancer Center, Amarillo, Texas
University of Texas Medical Branch, Galveston, Texas
University of Texas - MD Anderson Cancer Center, Houston, Texas
Wilford Hall Medical Center, Lackland Air Force Base, Texas
Joe Arrington Cancer Research and Treatment Center, Lubbock, Texas
Bayshore Medical Center, Pasadena, Texas
Dixie Regional Medical Center, Saint George, Utah
University of Utah Health Sciences Center, Salt Lake City, Utah
Latter Day Saints Hospital, Salt Lake City, Utah
Vermont Cancer Center, Burlington, Vermont
Cancer Center at the University of Virginia, Charlottesville, Virginia
RMH Regional Cancer Center, Harrisonburg, Virginia
Naval Medical Center, Portsmouth, Portsmouth, Virginia
Bon Secours - St. Mary's Hospital, Richmond, Virginia
Massey Cancer Center, Richmond, Virginia
Virginia Mason Medical Center, Seattle, Washington
Deaconess Medical Center, Spokane, Washington
Yakima Valley Memorial Hospital, Yakima, Washington
Schiffler Cancer Center, Wheeling, West Virginia
CCOP - St. Vincent Hospital Cancer Center, Green Bay, Green Bay, Wisconsin
St. Vincent Hospital, Green Bay, Wisconsin
Gundersen Lutheran Medical Foundation, La Crosse, Wisconsin
Southern Wisconsin Radiotherapy Center, Madison, Wisconsin
University of Wisconsin Comprehensive Cancer Center, Madison, Wisconsin
Marshfield Clinic, Marshfield, Wisconsin
Community Memorial Hospital, Menomonee Falls, Wisconsin
Columbia Hospital, Milwaukee, Wisconsin
St. Luke's Medical Center, Milwaukee, Wisconsin
Medical College of Wisconsin, Milwaukee, Wisconsin
Veterans Affairs Medical Center - Milwaukee (Zablocki), Milwaukee, Wisconsin
All Saints Cancer Center, Racine, Wisconsin
Waukesha Memorial Hospital, Waukesha, Wisconsin
Tom Baker Cancer Center - Calgary, Calgary, Alberta
Cross Cancer Institute, Edmonton, Alberta
Saint John Regional Hospital, Saint John, New Brunswick
Newfoundland Cancer Treatment and Research Foundation, St. Johns, Newfoundland and Labrador
Nova Scotia Cancer Centre, Halifax, Nova Scotia
Cancer Care Ontario-Hamilton Regional Cancer Centre, Hamilton, Ontario
Kingston Regional Cancer Centre, Kingston, Ontario
Cancer Care Ontario-London Regional Cancer Centre, London, Ontario
Ottawa Regional Cancer Centre, Ottawa, Ontario
Northeastern Ontario Regional Cancer Centre, Sudbury, Sudbury, Ontario
Northwestern Ontario Regional Cancer Centre, Thunder Bay, Thunder Bay, Ontario
Toronto Sunnybrook Regional Cancer Centre, Toronto, Ontario
Princess Margaret Hospital, Toronto, Ontario
CHUS-Hopital Fleurimont, Fleurimont, Quebec
Centre Hospitalier de l'Universite de Montreal, Montreal, Quebec
McGill University, Montreal, Quebec
Centre Hospitalier Universitaire de Quebec, Quebec City, Quebec
Allan Blair Cancer Centre, Regina, Saskatchewan
Saskatoon Cancer Centre, Saskatoon, Saskatchewan
Conditions: Head and Neck Cancer
Chemotherapy and Radiation Therapy Following Surgery in Treating Patients With Head and Neck Cancer
Completed
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Combining chemotherapy with radiation therapy following surgery may kill more tumor cells.
PURPOSE: Phase II trial to study the effectiveness of chemotherapy plus radiation therapy in treating patients who have undergone surgery for stage III or stage IV head and neck cancer.
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Combining chemotherapy with radiation therapy following surgery may kill more tumor cells.
PURPOSE: Phase II trial to study the effectiveness of chemotherapy plus radiation therapy in treating patients who have undergone surgery for stage III or stage IV head and neck cancer. Read Less
Gender:
ALL
Ages:
21 years and above
Trial Updated:
11/14/2015
Locations: University of Alabama at Birmingham Comprehensive Cancer Center, Birmingham, Alabama +233 locations
University of Alabama at Birmingham Comprehensive Cancer Center, Birmingham, Alabama
Comprehensive Cancer Institute of Huntsville, Huntsville, Alabama
Huntsville Hospital System, Huntsville, Alabama
MBCCOP - Gulf Coast, Mobile, Alabama
Alabama Oncology, LLC, Montgomery, Alabama
DCH Cancer Treatment Center, Tuscaloosa, Alabama
Foundation for Cancer Research and Education, Phoenix, Arizona
Mount Diablo Medical Center, Concord, California
City of Hope Comprehensive Cancer Center, Duarte, California
Saint Agnes Cancer Center, Fresno, California
California Cancer Center, Fresno, California
Sutter Health West Cancer Research Group, Greenbrae, California
Loma Linda University Medical Center, Loma Linda, California
Veterans Affairs Medical Center - Long Beach, Long Beach, California
Jonsson Comprehensive Cancer Center, UCLA, Los Angeles, California
USC/Norris Comprehensive Cancer Center and Hospital, Los Angeles, California
CCOP - Bay Area Tumor Institute, Oakland, California
Huntington Cancer Center, Pasadena, California
Robert and Beverly Lewis Family Cancer Care Center, Pomona, California
Radiation Oncology Center - Sacramento, Sacramento, California
Radiation Medical Group, Inc., San Diego, California
UCSF Comprehensive Cancer Center, San Francisco, California
O'Connor Hospital, San Jose, California
CCOP - Santa Rosa Memorial Hospital, Santa Rosa, California
David Grant Medical Center, Travis Air Force Base, California
Memorial Hospital Cancer Center, Colorado Springs, Colorado
University of Colorado Cancer Center, Denver, Colorado
Saint Mary's Hospital and Medical Center, Grand Junction, Colorado
Hospital of St. Raphael, New Haven, Connecticut
CCOP - Christiana Care Health Services, Wilmington, Delaware
University of Florida Health Science Center, Gainesville, Florida
Florida Radiation Oncology Group, Jacksonville, Florida
Health First Holmes Regional Medical Center, Melbourne, Florida
CCOP - Mount Sinai Medical Center, Miami Beach, Florida
Veterans Affairs Medical Center - Miami, Miami, Florida
Sylvester Cancer Center, University of Miami, Miami, Florida
Baptist Hospital of Miami, Miami, Florida
MD Anderson Cancer Center Orlando, Orlando, Florida
Bay Medical Center, Panama City, Florida
Gulf Coast Cancer Treatment Center, Panama City, Florida
Sarasota Radiation and Medical Oncology Center, Sarasota, Florida
Tallahassee Memorial Healthcare, Tallahassee, Florida
H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida
Emory University Hospital - Atlanta, Atlanta, Georgia
CCOP - Atlanta Regional, Atlanta, Georgia
Medical Center/John B. Amos Community Cancer Center, Columbus, Georgia
Regional Radiation Oncology Center at Rome, Rome, Georgia
MBCCOP - Hawaii, Honolulu, Hawaii
Northwest Community Hospital, Arlington Heights, Illinois
Northwestern Memorial Hospital, Chicago, Illinois
CCOP - Central Illinois, Decatur, Illinois
Ingalls Memorial Hospital, Harvey, Illinois
Loyola University Medical Center, Maywood, Illinois
Lutheran General Cancer Care Center, Park Ridge, Illinois
Methodist Medical Center of Illinois, Peoria, Illinois
St. John's Medical Center, Anderson, Indiana
Bloomington Hospital, Bloomington, Indiana
Veterans Affairs Medical Center - Indianapolis (Roudebush), Indianapolis, Indiana
Clarian Health Partners Inc., Indianapolis, Indiana
Regional Cancer Center, Indianapolis, Indiana
Ball Memorial Hospital, Muncie, Indiana
CCOP - Northern Indiana CR Consortium, South Bend, Indiana
Wendt Regional Cancer Center of Finley Hospital, Dubuque, Iowa
Central Baptist Hospital, Lexington, Kentucky
Albert B. Chandler Medical Center, University of Kentucky, Lexington, Kentucky
James Graham Brown Cancer Center, Louisville, Kentucky
Louisville Radiation Oncology, Louisville, Kentucky
Merle M. Mahr Cancer Center, Madisonville, Kentucky
Mary Bird Perkins Cancer Center, Baton Rouge, Louisiana
Tulane University School of Medicine, New Orleans, Louisiana
MBCCOP - LSU Medical Center, New Orleans, Louisiana
CCOP - Ochsner, New Orleans, Louisiana
Maine Medical Center, Portland, Maine
Anne Arundel Oncology Center, Annapolis, Maryland
Marlene and Stewart Greenebaum Cancer Center, University of Maryland, Baltimore, Maryland
Greater Baltimore Medical Center and Cancer Center, Baltimore, Maryland
Harbor Hospital Center, Baltimore, Maryland
Sinai Hospital of Baltimore, Baltimore, Maryland
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland
Peninsula Regional Medical Center, Salisbury, Maryland
Dana-Farber Cancer Institute, Boston, Massachusetts
Cape Cod Hospital, Hyannis, Massachusetts
Veterans Affairs Medical Center - Boston (Jamaica Plain), Jamaica Plain, Massachusetts
CCOP - Ann Arbor Regional, Ann Arbor, Michigan
University of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan
Barbara Ann Karmanos Cancer Institute, Detroit, Michigan
Henry Ford Hospital, Detroit, Michigan
Hurley Medical Center, Flint, Michigan
McLaren Regional Cancer Center, Flint, Michigan
CCOP - Kalamazoo, Kalamazoo, Michigan
Marquette General Hospital, Marquette, Michigan
MidMichigan Medical Center - Midland, Midland, Michigan
CCOP - Beaumont, Royal Oak, Michigan
William Beaumont Hospital, Royal Oak, Michigan
William Beaumont Hospital - Troy, Troy, Michigan
Mayo Clinic Cancer Center, Rochester, Minnesota
CCOP - Metro-Minnesota, Saint Louis Park, Minnesota
Ellis Fischel Cancer Center - Columbia, Columbia, Missouri
CCOP - Kansas City, Kansas City, Missouri
Mallinckrodt Institute of Radiology, Saint Louis, Missouri
St. Louis University Health Sciences Center, Saint Louis, Missouri
Cancer Research for the Ozarks, Springfield, Missouri
CCOP - Cancer Research for the Ozarks, Springfield, Missouri
CCOP - Montana Cancer Consortium, Billings, Montana
CCOP - Missouri Valley Cancer Consortium, Omaha, Nebraska
Methodist Hospital Cancer Center - Omaha, Omaha, Nebraska
Nebraska Health System, Omaha, Nebraska
CCOP - Southern Nevada Cancer Research Foundation, Las Vegas, Nevada
Norris Cotton Cancer Center, Lebanon, New Hampshire
Elliot Regional Cancer Center, Manchester, New Hampshire
Veterans Affairs Medical Center - East Orange, East Orange, New Jersey
John F. Kennedy Medical Center, Edison, New Jersey
Trinitas Hospital - Jersey Street Campus, Elizabeth, New Jersey
Monmouth Medical Center, Long Branch, New Jersey
South Jersey Regional Cancer Center, Millville, New Jersey
Fox Chase Virtua Health Cancer Program at Virtua Memorial Hospital, Mount Holly, New Jersey
Cancer Institute of New Jersey, New Brunswick, New Jersey
Newark Beth Israel Medical Center, Newark, New Jersey
Atlantic City Medical Center, Pomona, New Jersey
Valley Hospital, Ridgewood, New Jersey
Community Medical Center, Toms River, New Jersey
St. Francis Medical Center, Trenton, New Jersey
Associated Radiologists, P.A., Warren, New Jersey
Radiation Oncology Associates of Albuquerque, Albuquerque, New Mexico
Cancer Center of Albany Medical Center, Albany, New York
State University of New York Health Science Center at Brooklyn, Brooklyn, New York
New York Methodist Hospital, Brooklyn, New York
Roswell Park Cancer Institute, Buffalo, New York
Finger Lakes Radiation Oncology Center, Clifton Springs, New York
CCOP - North Shore University Hospital, Manhasset, New York
Herbert Irving Comprehensive Cancer Center, New York, New York
Champlain Valley Physicians Hospital Medical Center, Plattsburgh, New York
Vassar Brothers Medical Center, Poughkeepsie, New York
James P. Wilmot Cancer Center, Rochester, New York
CCOP - Syracuse Hematology-Oncology Associates of Central New York, P.C., Syracuse, New York
Riverhill Radiation Oncology, Yonkers, New York
Lineberger Comprehensive Cancer Center, UNC, Chapel Hill, North Carolina
Northeast Medical Center, Concord, North Carolina
East Carolina University School of Medicine, Greenville, North Carolina
CCOP - Southeast Cancer Control Consortium, Winston-Salem, North Carolina
Comprehensive Cancer Center at Wake Forest University, Winston-Salem, North Carolina
Trinity Cancer Care Center, Minot, North Dakota
Akron General Medical Center, Akron, Ohio
Akron City Hospital, Akron, Ohio
Christ Hospital, Cincinnati, Ohio
Barrett Cancer Center, Cincinnati, Ohio
Ireland Cancer Center, Cleveland, Ohio
University Hospitals of Cleveland, Cleveland, Ohio
Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio
CCOP - Columbus, Columbus, Ohio
Arthur G. James Cancer Hospital - Ohio State University, Columbus, Ohio
CCOP - Dayton, Dayton, Ohio
CCOP - Toledo Community Hospital, Toledo, Ohio
St. Anthony Hospital, Oklahoma City, Oklahoma
University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma
St. John Health System, Tulsa, Oklahoma
CCOP - Oklahoma, Tulsa, Oklahoma
CCOP - Columbia River Program, Portland, Oregon
Lehigh Valley Hospital, Allentown, Pennsylvania
St. Luke's Hospital Cancer Center, Bethlehem, Pennsylvania
Geisinger Medical Center, Danville, Pennsylvania
Mercy Fitzgerald Hospital, Darby, Pennsylvania
Delaware County Memorial Hospital, Drexel Hill, Pennsylvania
Pocono Cancer Center, East Stroudsburg, Pennsylvania
Milton S. Hershey Medical Center, Hershey, Pennsylvania
University of Pennsylvania Cancer Center, Philadelphia, Pennsylvania
Veterans Affairs Medical Center - Philadelphia, Philadelphia, Pennsylvania
Kimmel Cancer Center of Thomas Jefferson University - Philadelphia, Philadelphia, Pennsylvania
Fox Chase Cancer Center, Philadelphia, Pennsylvania
Albert Einstein Cancer Center, Philadelphia, Pennsylvania
University of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania
Mercy Hospital of Pittsburgh, Pittsburgh, Pennsylvania
Western Pennsylvania Hospital, Pittsburgh, Pennsylvania
Reading Hospital and Medical Center, Reading, Pennsylvania
Mercy Hospital Cancer Center - Scranton, Scranton, Pennsylvania
Wilkes Barre General Hospital, Wilkes-Barre, Pennsylvania
York Cancer Center, York, Pennsylvania
Roger Williams Medical Center/BUSM, Providence, Rhode Island
CCOP - Greenville, Greenville, South Carolina
CCOP - Upstate Carolina, Spartanburg, South Carolina
Rapid City Regional Hospital, Rapid City, South Dakota
Jackson-Madison County General Hospital, Jackson, Tennessee
University of Tennessee Cancer Institute, Memphis, Tennessee
Vanderbilt-Ingram Cancer Center, Nashville, Tennessee
Harrington Cancer Center, Amarillo, Texas
University of Texas Medical Branch, Galveston, Texas
University of Texas - MD Anderson Cancer Center, Houston, Texas
Wilford Hall Medical Center, Lackland Air Force Base, Texas
Joe Arrington Cancer Research and Treatment Center, Lubbock, Texas
Dixie Regional Medical Center, Saint George, Utah
University of Utah Health Sciences Center, Salt Lake City, Utah
Latter Day Saints Hospital, Salt Lake City, Utah
Vermont Cancer Center, Burlington, Vermont
Cancer Center at the University of Virginia, Charlottesville, Virginia
RMH Regional Cancer Center, Harrisonburg, Virginia
Naval Medical Center, Portsmouth, Portsmouth, Virginia
Bon Secours - St. Mary's Hospital, Richmond, Virginia
Massey Cancer Center, Richmond, Virginia
Virginia Mason Medical Center, Seattle, Washington
Deaconess Medical Center, Spokane, Washington
Yakima Valley Memorial Hospital, Yakima, Washington
Schiffler Cancer Center, Wheeling, West Virginia
CCOP - St. Vincent Hospital Cancer Center, Green Bay, Green Bay, Wisconsin
St. Vincent Hospital, Green Bay, Wisconsin
Gundersen Lutheran Medical Foundation, La Crosse, Wisconsin
Southern Wisconsin Radiotherapy Center, Madison, Wisconsin
University of Wisconsin Comprehensive Cancer Center, Madison, Wisconsin
Marshfield Clinic, Marshfield, Wisconsin
Community Memorial Hospital, Menomonee Falls, Wisconsin
Columbia Hospital, Milwaukee, Wisconsin
St. Luke's Medical Center, Milwaukee, Wisconsin
Medical College of Wisconsin, Milwaukee, Wisconsin
Veterans Affairs Medical Center - Milwaukee (Zablocki), Milwaukee, Wisconsin
All Saints Cancer Center, Racine, Wisconsin
Waukesha Memorial Hospital, Waukesha, Wisconsin
Tom Baker Cancer Center - Calgary, Calgary, Alberta
Cross Cancer Institute, Edmonton, Alberta
Saint John Regional Hospital, Saint John, New Brunswick
Newfoundland Cancer Treatment and Research Foundation, St. Johns, Newfoundland and Labrador
Nova Scotia Cancer Centre, Halifax, Nova Scotia
Cancer Care Ontario-Hamilton Regional Cancer Centre, Hamilton, Ontario
Kingston Regional Cancer Centre, Kingston, Ontario
Cancer Care Ontario-London Regional Cancer Centre, London, Ontario
Ottawa Regional Cancer Centre, Ottawa, Ontario
Northeastern Ontario Regional Cancer Centre, Sudbury, Sudbury, Ontario
Northwestern Ontario Regional Cancer Centre, Thunder Bay, Thunder Bay, Ontario
Toronto Sunnybrook Regional Cancer Centre, Toronto, Ontario
Princess Margaret Hospital, Toronto, Ontario
CHUS-Hopital Fleurimont, Fleurimont, Quebec
Centre Hospitalier de l'Universite de Montreal, Montreal, Quebec
McGill University, Montreal, Quebec
Centre Hospitalier Universitaire de Quebec, Quebec City, Quebec
Allan Blair Cancer Centre, Regina, Saskatchewan
Saskatoon Cancer Centre, Saskatoon, Saskatchewan
Conditions: Head and Neck Cancer
Ascending Multiple-Dose Study of Brivanib Alaninate in Combination With Chemotherapeutic Agents in Subjects With Advanced Cancers
Completed
To determine safety and maximum tolerated dose of brivanib alaninate when administered in combination with capecitabine, doxorubicin, ixabepilone, docetaxel and paclitaxel chemotherapy to subjects with advanced or metastatic solid tumors
To determine safety and maximum tolerated dose of brivanib alaninate when administered in combination with capecitabine, doxorubicin, ixabepilone, docetaxel and paclitaxel chemotherapy to subjects with advanced or metastatic solid tumors Read Less
Gender:
ALL
Ages:
Between 18 years and 75 years
Trial Updated:
07/03/2015
Locations: Usc/Norris Comprehensive Cancer Center, Los Angeles, California +4 locations
Usc/Norris Comprehensive Cancer Center, Los Angeles, California
Dana Farber Cancer Institute, Boston, Massachusetts
Wayne State University, Detroit, Michigan
Local Institution, Edmonton, Alberta
Local Institution, Toronto, Ontario
Conditions: Advanced Cancer
Paclitaxel With / Without GW572016 (Lapatinib) As First Line Therapy For Women With Advanced Or Metastatic Breast Cancer
Completed
The purpose of this study is to determine the efficacy and safety of an oral dual tyrosine kinase inhibitor (GW572016) in combination with paclitaxel compared to paclitaxel alone in first line advanced or metastatic breast cancer.
The purpose of this study is to determine the efficacy and safety of an oral dual tyrosine kinase inhibitor (GW572016) in combination with paclitaxel compared to paclitaxel alone in first line advanced or metastatic breast cancer. Read Less
Gender:
FEMALE
Ages:
18 years and above
Trial Updated:
04/16/2015
Locations: GSK Investigational Site, Tucson, Arizona +176 locations
GSK Investigational Site, Tucson, Arizona
GSK Investigational Site, Hot Springs, Arkansas
GSK Investigational Site, Jonesboro, Arkansas
GSK Investigational Site, Fountain Valley, California
GSK Investigational Site, La Jolla, California
GSK Investigational Site, Rancho Mirage, California
GSK Investigational Site, Vallejo, California
GSK Investigational Site, Denver, Colorado
GSK Investigational Site, Boca Raton, Florida
GSK Investigational Site, Orlando, Florida
GSK Investigational Site, Port St. Lucie, Florida
GSK Investigational Site, West Palm Beach, Florida
GSK Investigational Site, Atlanta, Georgia
GSK Investigational Site, Marietta, Georgia
GSK Investigational Site, Savannah, Georgia
GSK Investigational Site, Savannah, Georgia
GSK Investigational Site, Indianapolis, Indiana
GSK Investigational Site, Kansas City, Kansas
GSK Investigational Site, Metairie, Louisiana
GSK Investigational Site, Baltimore, Maryland
GSK Investigational Site, Glen Burnie, Maryland
GSK Investigational Site, Springfield, Massachusetts
GSK Investigational Site, Duluth, Minnesota
GSK Investigational Site, Robbinsdale, Minnesota
GSK Investigational Site, St. Louis, Missouri
GSK Investigational Site, Voorhees, New Jersey
GSK Investigational Site, Santa Fe, New Mexico
GSK Investigational Site, Nyack, New York
GSK Investigational Site, Syracuse, New York
GSK Investigational Site, Charlotte, North Carolina
GSK Investigational Site, Greenville, North Carolina
GSK Investigational Site, Fargo, North Dakota
GSK Investigational Site, Canton, Ohio
GSK Investigational Site, Portland, Oregon
GSK Investigational Site, Columbia, South Carolina
GSK Investigational Site, Knoxville, Tennessee
GSK Investigational Site, Knoxville, Tennessee
GSK Investigational Site, Amarillo, Texas
GSK Investigational Site, Fort Worth, Texas
GSK Investigational Site, Houston, Texas
GSK Investigational Site, San Antonio, Texas
GSK Investigational Site, Burlington, Vermont
GSK Investigational Site, Norfolk, Virginia
GSK Investigational Site, Tacoma, Washington
GSK Investigational Site, Milwaukee, Wisconsin
GSK Investigational Site, Capital Federal, Buenos Aires
GSK Investigational Site, Capital Federal, Buenos Aires
GSK Investigational Site, Buenos Aires, Not set
GSK Investigational Site, Fitzroy, Victoria
GSK Investigational Site, Malvern, Victoria
GSK Investigational Site, Wodonga, Victoria
GSK Investigational Site, Nedlands, Western Australia
GSK Investigational Site, Vienna, Not set
GSK Investigational Site, Brugge, Not set
GSK Investigational Site, Brussels, Not set
GSK Investigational Site, Brussel, Not set
GSK Investigational Site, Kortrijk, Not set
GSK Investigational Site, Leuven, Not set
GSK Investigational Site, Roeselare, Not set
GSK Investigational Site, Salvador, Bahía
GSK Investigational Site, Rio de Janeiro, Not set
GSK Investigational Site, Saint John's, Newfoundland and Labrador
GSK Investigational Site, Sudbury, Ontario
GSK Investigational Site, Thunder Bay, Ontario
GSK Investigational Site, Montreal, Quebec
GSK Investigational Site, Montreal, Quebec
GSK Investigational Site, Sherbrooke, Quebec
GSK Investigational Site, Santiago, Región Metro De Santiago
GSK Investigational Site, Santiago, Región Metro De Santiago
GSK Investigational Site, Santiago, Región Metro De Santiago
GSK Investigational Site, Brno, Not set
GSK Investigational Site, Hradec Kralove, Not set
GSK Investigational Site, Olomouc, Not set
GSK Investigational Site, Aalen, Baden-Wuerttemberg
GSK Investigational Site, Stuttgart, Baden-Wuerttemberg
GSK Investigational Site, Ulm, Baden-Wuerttemberg
GSK Investigational Site, Augsburg, Bayern
GSK Investigational Site, Bayreuth, Bayern
GSK Investigational Site, Coburg, Bayern
GSK Investigational Site, Muenchen, Bayern
GSK Investigational Site, Muenchen, Bayern
GSK Investigational Site, Fuerstenwalde, Brandenburg
GSK Investigational Site, Stade, Niedersachsen
GSK Investigational Site, Herne, Nordrhein-Westfalen
GSK Investigational Site, Ibbenbueren, Nordrhein-Westfalen
GSK Investigational Site, Muenster, Nordrhein-Westfalen
GSK Investigational Site, Halle, Sachsen-Anhalt
GSK Investigational Site, Kiel, Schleswig-Holstein
GSK Investigational Site, Jena, Thueringen
GSK Investigational Site, Berlin, Not set
GSK Investigational Site, Berlin, Not set
GSK Investigational Site, Berlin, Not set
GSK Investigational Site, Berlin, Not set
GSK Investigational Site, Hamburg, Not set
GSK Investigational Site, Hamburg, Not set
GSK Investigational Site, Hamburg, Not set
GSK Investigational Site, Budapest, Not set
GSK Investigational Site, Nyíregyháza, Not set
GSK Investigational Site, Szombathely, Not set
GSK Investigational Site, Zalaegerszeg-Pózva, Not set
GSK Investigational Site, Benevento, Campania
GSK Investigational Site, Napoli, Campania
GSK Investigational Site, Forlì, Emilia-Romagna
GSK Investigational Site, Parma, Emilia-Romagna
GSK Investigational Site, Ravenna, Emilia-Romagna
GSK Investigational Site, Rimini, Emilia-Romagna
GSK Investigational Site, Roma, Lazio
GSK Investigational Site, Roma, Lazio
GSK Investigational Site, Pietra Ligure (SV), Liguria
GSK Investigational Site, Bergamo, Lombardia
GSK Investigational Site, Pavia, Lombardia
GSK Investigational Site, Candiolo (TO), Piemonte
GSK Investigational Site, Torino, Piemonte
GSK Investigational Site, Sassari, Sardegna
GSK Investigational Site, Prato (PO), Toscana
GSK Investigational Site, Perugia, Umbria
GSK Investigational Site, Gyeonggi-do, Not set
GSK Investigational Site, Seoul, Not set
GSK Investigational Site, Daugavpils, Not set
GSK Investigational Site, Liepaja, Not set
GSK Investigational Site, Riga, Not set
GSK Investigational Site, Riga, Not set
GSK Investigational Site, Acapulco, Guerrero
GSK Investigational Site, Guadalajara, Jalisco
GSK Investigational Site, Colima, Not set
GSK Investigational Site, Durango, Not set
GSK Investigational Site, Amersfoort, Not set
GSK Investigational Site, Leiden, Not set
GSK Investigational Site, Nieuwegein, Not set
GSK Investigational Site, Utrecht, Not set
GSK Investigational Site, Utrecht, Not set
GSK Investigational Site, Auckland, Not set
GSK Investigational Site, Christchurch, Not set
GSK Investigational Site, Lahore, Not set
GSK Investigational Site, Lahore, Not set
GSK Investigational Site, Callao, Not set
GSK Investigational Site, Lima, Not set
GSK Investigational Site, Krakow, Not set
GSK Investigational Site, Olsztyn, Not set
GSK Investigational Site, Olsztyn, Not set
GSK Investigational Site, Poznan, Not set
GSK Investigational Site, Warszawa, Not set
GSK Investigational Site, Wroclaw, Not set
GSK Investigational Site, Moscow Region, Not set
GSK Investigational Site, Moscow, Not set
GSK Investigational Site, Moscow, Not set
GSK Investigational Site, Moscow, Not set
GSK Investigational Site, Moscow, Not set
GSK Investigational Site, Moscow, Not set
GSK Investigational Site, St. Petersburg, Not set
GSK Investigational Site, St. Petersburg, Not set
GSK Investigational Site, Banska Bystrica, Not set
GSK Investigational Site, Bratislava, Not set
GSK Investigational Site, Kosice, Not set
GSK Investigational Site, Poprad, Not set
GSK Investigational Site, Parktown, Gauteng
GSK Investigational Site, Capital Park, Not set
GSK Investigational Site, Overport, Not set
GSK Investigational Site, Parow, Not set
GSK Investigational Site, Port Elizabeth, Not set
GSK Investigational Site, Alcorcón/Madrid, Not set
GSK Investigational Site, Baracaldo/Vizcaya, Not set
GSK Investigational Site, Caceres, Not set
GSK Investigational Site, Cuidad Real, Not set
GSK Investigational Site, Jaen, Not set
GSK Investigational Site, La Laguna (Santa Cruz de Tenerife), Not set
GSK Investigational Site, Las Palmas De Gran Canaria, Not set
GSK Investigational Site, Madrid, Not set
GSK Investigational Site, Móstoles/Madrid, Not set
GSK Investigational Site, Palma de Mallorca, Not set
GSK Investigational Site, Pontevedra, Not set
GSK Investigational Site, San Sebastián, Not set
GSK Investigational Site, Santa Cruz de Tenerife, Not set
GSK Investigational Site, Zaragoza, Not set
GSK Investigational Site, Zaragoza, Not set
GSK Investigational Site, Istanbul, Not set
GSK Investigational Site, Istanbul, Not set
Conditions: Neoplasms, Breast
Trial of Paclitaxel/Carboplatin + PF-3512676 vs Paclitaxel/Carboplatin Alone in Patients With Advanced Non-Small Cell Lung Cancer
Terminated
To assess the efficacy and safety of PF-3512676 administered in combination with paclitaxel/carboplatin chemotherapy as first-line treatment in patients with locally advanced or metastatic Non-Small-Cell Lung Cancer (NSCLC) and to compare it to the efficacy and safety of paclitaxel
To assess the efficacy and safety of PF-3512676 administered in combination with paclitaxel/carboplatin chemotherapy as first-line treatment in patients with locally advanced or metastatic Non-Small-Cell Lung Cancer (NSCLC) and to compare it to the efficacy and safety of paclitaxel Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
03/10/2015
Locations: Pfizer Investigational Site, Little Rock, Alaska +190 locations
Pfizer Investigational Site, Little Rock, Alaska
Pfizer Investigational Site, Hot Springs, Arkansas
Pfizer Investigational Site, Chula Vista, California
Pfizer Investigational Site, La Mesa, California
Pfizer Investigational Site, Oceanside, California
Pfizer Investigational Site, Palm Springs, California
Pfizer Investigational Site, San Diego, California
Pfizer Investigational Site, San Francisco, California
Pfizer Investigational Site, Atlanta, Georgia
Pfizer Investigational Site, Atlanta, Georgia
Pfizer Investigational Site, Atlanta, Georgia
Pfizer Investigational Site, Atlanta, Georgia
Pfizer Investigational Site, Atlanta, Georgia
Pfizer Investigational Site, Decatur, Georgia
Pfizer Investigational Site, Fayetteville, Georgia
Pfizer Investigational Site, Macon, Georgia
Pfizer Investigational Site, Marietta, Georgia
Pfizer Investigational Site, Tucker, Georgia
Pfizer Investigational Site, Rockford, Illinois
Pfizer Investigational Site, Jefferson, Indiana
Pfizer Investigational Site, New Albany, Indiana
Pfizer Investigational Site, Cedar Rapids, Iowa
Pfizer Investigational Site, Dubuque, Iowa
Pfizer Investigational Site, Lexington, Kentucky
Pfizer Investigational Site, Louisville, Kentucky
Pfizer Investigational Site, Louisville, Kentucky
Pfizer Investigational Site, Louisville, Kentucky
Pfizer Investigational Site, Louisville, Kentucky
Pfizer Investigational Site, Shelbyville, Kentucky
Pfizer Investigational Site, Covington, Louisiana
Pfizer Investigational Site, Gretna, Louisiana
Pfizer Investigational Site, Lafayette, Louisiana
Pfizer Investigational Site, Marrero, Louisiana
Pfizer Investigational Site, Marrero, Louisiana
Pfizer Investigational Site, Metairie, Louisiana
Pfizer Investigational Site, New Orleans, Louisiana
Pfizer Investigational Site, Biddeford, Maine
Pfizer Investigational Site, Brunswick, Maine
Pfizer Investigational Site, Scarborough, Maine
Pfizer Investigational Site, Worcester, Massachusetts
Pfizer Investigational Site, Allegan, Michigan
Pfizer Investigational Site, Ann Arbor, Michigan
Pfizer Investigational Site, Ann Arbor, Michigan
Pfizer Investigational Site, Kalamazoo, Michigan
Pfizer Investigational Site, Kalamazoo, Michigan
Pfizer Investigational Site, St. Joseph, Michigan
Pfizer Investigational Site, Columbus, Mississippi
Pfizer Investigational Site, Corinth, Mississippi
Pfizer Investigational Site, Tupelo, Mississippi
Pfizer Investigational Site, Omaha, Nebraska
Pfizer Investigational Site, Omaha, Nebraska
Pfizer Investigational Site, Omaha, Nebraska
Pfizer Investigational Site, Papillion, Nebraska
Pfizer Investigational Site, Las Vegas, Nevada
Pfizer Investigational Site, Las Vegas, Nevada
Pfizer Investigational Site, Albuquerque, New Mexico
Pfizer Investigational Site, Ruidoso, New Mexico
Pfizer Investigational Site, Buffalo, New York
Pfizer Investigational Site, Great Neck, New York
Pfizer Investigational Site, Asheville, North Carolina
Pfizer Investigational Site, Brevard, North Carolina
Pfizer Investigational Site, Lexington, North Carolina
Pfizer Investigational Site, Winston-Salem, North Carolina
Pfizer Investigational Site, Canton, Ohio
Pfizer Investigational Site, Dover, Ohio
Pfizer Investigational Site, Oklahoma City, Oklahoma
Pfizer Investigational Site, Portland, Oregon
Pfizer Investigational Site, Langhorne, Pennsylvania
Pfizer Investigational Site, Chattanooga, Tennessee
Pfizer Investigational Site, Memphis, Tennessee
Pfizer Investigational Site, Arlington, Texas
Pfizer Investigational Site, Dallas, Texas
Pfizer Investigational Site, Dallas, Texas
Pfizer Investigational Site, Dallas, Texas
Pfizer Investigational Site, Dallas, Texas
Pfizer Investigational Site, Dallas, Texas
Pfizer Investigational Site, Richardson, Texas
Pfizer Investigational Site, Trophy Club, Texas
Pfizer Investigational Site, Bountiful, Utah
Pfizer Investigational Site, Layton, Utah
Pfizer Investigational Site, Murray, Utah
Pfizer Investigational Site, Provo, Utah
Pfizer Investigational Site, Salt Lake City, Utah
Pfizer Investigational Site, WVC, Utah
Pfizer Investigational Site, Burlington, Vermont
Pfizer Investigational Site, Everett, Washington
Pfizer Investigational Site, Kennewick, Washington
Pfizer Investigational Site, Richland, Washington
Pfizer Investigational Site, Madison, Wisconsin
Pfizer Investigational Site, Albury, New South Wales
Pfizer Investigational Site, Camperdown, New South Wales
Pfizer Investigational Site, Randwick, New South Wales
Pfizer Investigational Site, Pimlico, Queensland
Pfizer Investigational Site, Townsville, Queensland
Pfizer Investigational Site, Woolloongabba, Queensland
Pfizer Investigational Site, Bedford Park, South Australia
Pfizer Investigational Site, Toorak Gardens, South Australia
Pfizer Investigational Site, East Melbourne, Victoria
Pfizer Investigational Site, East Ringwood, Victoria
Pfizer Investigational Site, Wodonga, Victoria
Pfizer Investigational Site, Nedlands, Western Australia
Pfizer Investigational Site, Gent, Not set
Pfizer Investigational Site, Liège, Not set
Pfizer Investigational Site, Moncton, New Brunswick
Pfizer Investigational Site, Montreal, Quebec
Pfizer Investigational Site, Montreal, Quebec
Pfizer Investigational Site, Montreal, Quebec
Pfizer Investigational Site, Montreal, Quebec
Pfizer Investigational Site, Rimouski, Quebec
Pfizer Investigational Site, Saskatoon, Saskatchewan
Pfizer Investigational Site, Dalian, Xigang District, Liaoning
Pfizer Investigational Site, Beijing, Not set
Pfizer Investigational Site, Beijing, Not set
Pfizer Investigational Site, Shanghai, Not set
Pfizer Investigational Site, Nicosia, Not set
Pfizer Investigational Site, Nova Ves Pod Plesi, Not set
Pfizer Investigational Site, Ostrava-Poruba, Not set
Pfizer Investigational Site, Usti nad Labem, Not set
Pfizer Investigational Site, Angers cedex, Not set
Pfizer Investigational Site, Caen cedex, Not set
Pfizer Investigational Site, Dijon, Not set
Pfizer Investigational Site, Limoges, Not set
Pfizer Investigational Site, Nantes Cedex 2, Not set
Pfizer Investigational Site, Paris Cedex 13, Not set
Pfizer Investigational Site, St Herblain Cedex, Not set
Pfizer Investigational Site, Strasbourg, Not set
Pfizer Investigational Site, Toulouse cedex 9, Not set
Pfizer Investigational Site, Vandoeuvre Les Nancy, Not set
Pfizer Investigational Site, Berlin, Not set
Pfizer Investigational Site, Bielefeld, Not set
Pfizer Investigational Site, Bonn, Not set
Pfizer Investigational Site, Essen, Not set
Pfizer Investigational Site, Frankfurt, Not set
Pfizer Investigational Site, Karlsruhe, Not set
Pfizer Investigational Site, Muenchen, Not set
Pfizer Investigational Site, Athens, Attica
Pfizer Investigational Site, Heraklion, Crete
Pfizer Investigational Site, Thessaloniki, Macedonia
Pfizer Investigational Site, Athens, Not set
Pfizer Investigational Site, Rio, Patras, Not set
Pfizer Investigational Site, Pokfulam, Not set
Pfizer Investigational Site, Budapest, Not set
Pfizer Investigational Site, Budapest, Not set
Pfizer Investigational Site, Budapest, Not set
Pfizer Investigational Site, Debrecen, Not set
Pfizer Investigational Site, Bangalore, Karnataka
Pfizer Investigational Site, Kochi, Kerala
Pfizer Investigational Site, Pune, Maharashtra
Pfizer Investigational Site, Chandigarh, Punjab
Pfizer Investigational Site, Jaipur, Rajasthan
Pfizer Investigational Site, Zerifin, Not set
Pfizer Investigational Site, Lido di Camaiore (LU), Not set
Pfizer Investigational Site, Milano, Not set
Pfizer Investigational Site, Napoli, Not set
Pfizer Investigational Site, Pavia, Not set
Pfizer Investigational Site, Seoul, Not set
Pfizer Investigational Site, Seoul, Not set
Pfizer Investigational Site, Mexico, DF
Pfizer Investigational Site, Puebla, Not set
Pfizer Investigational Site, Tiel, GLD
Pfizer Investigational Site, Groningen, GR
Pfizer Investigational Site, Amstelveen, Not set
Pfizer Investigational Site, Den Haag, Not set
Pfizer Investigational Site, Otwock, Not set
Pfizer Investigational Site, Wodzislaw Sl., Not set
Pfizer Investigational Site, Faro, Not set
Pfizer Investigational Site, Porto, Not set
Pfizer Investigational Site, Porto, Not set
Pfizer Investigational Site, Vila Nova de Gaia, Not set
Pfizer Investigational Site, Parktown, Gauteng
Pfizer Investigational Site, Cape Town, Not set
Pfizer Investigational Site, Cape Town, Not set
Pfizer Investigational Site, Johannesburg, Not set
Pfizer Investigational Site, Badalona, Barcelona
Pfizer Investigational Site, Alcorcon, Madrid
Pfizer Investigational Site, Pamplona, Navarra
Pfizer Investigational Site, Madrid, Not set
Pfizer Investigational Site, Madrid, Not set
Pfizer Investigational Site, Santa Cruz de Tenerife, Not set
Pfizer Investigational Site, Valencia, Not set
Pfizer Investigational Site, Stockholm, Not set
Pfizer Investigational Site, Uppsala, Not set
Pfizer Investigational Site, Lausanne, Not set
Pfizer Investigational Site, Taipei, Not set
Pfizer Investigational Site, Truro, Cornwall
Pfizer Investigational Site, Exeter, Devon
Pfizer Investigational Site, London, Not set
Pfizer Investigational Site, Portsmouth, Not set
Pfizer Investigational Site, Sheffield, Not set
Pfizer Investigational Site, Surrey GU2 5XX, Not set
Pfizer Investigational Site, Swansea, Not set
Conditions: Carcinoma, Non-Small-Cell Lung
Paclitaxel Eluting Balloon for SFA In-stent Restenosis
Unknown
The purpose of the study is to evaluate the safety and efficacy on the use of drug eluting balloon (DEB) with paclitaxel to treat in-stent restenosis in femoropopliteal arteries.
The purpose of the study is to evaluate the safety and efficacy on the use of drug eluting balloon (DEB) with paclitaxel to treat in-stent restenosis in femoropopliteal arteries. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
12/05/2014
Locations: University Health Network, Toronto, Ontario
University Health Network, Toronto, Ontario
Conditions: In-stent Arterial Restenosis
A Study to Evaluate the Effect of the Combination of Pertuzumab With Carboplatin-Based Standard Chemotherapy in Patients With Recurrent Ovarian Cancer
Completed
This study will evaluate the efficacy and safety of pertuzumab in combination with carboplatin-based standard chemotherapy in patients with platinum-sensitive recurrent ovarian cancer. The anticipated time on study treatment is 3-12 months.
This study will evaluate the efficacy and safety of pertuzumab in combination with carboplatin-based standard chemotherapy in patients with platinum-sensitive recurrent ovarian cancer. The anticipated time on study treatment is 3-12 months. Read Less
Gender:
FEMALE
Ages:
18 years and above
Trial Updated:
11/25/2014
Locations: Not set, Bruxelles, Not set +33 locations
Not set, Bruxelles, Not set
Not set, Leuven, Not set
Not set, Wilrijk, Not set
Not set, Calgary, Alberta
Not set, Kelowna, British Columbia
Not set, Vancouver, British Columbia
Not set, Budapest, Not set
Not set, Debrecen, Not set
Not set, Gyor, Not set
Not set, Parma, Emilia-Romagna
Not set, Milano, Lombardia
Not set, Amsterdam, Not set
Not set, Amsterdam, Not set
Not set, Poznan, Not set
Not set, Warszawa, Not set
Not set, Kazan, Not set
Not set, Moscow, Not set
Not set, Moscow, Not set
Not set, Moscow, Not set
Not set, Moscow, Not set
Not set, Moscow, Not set
Not set, Saint-Petersburg, Not set
Not set, St Petersburg, Not set
Not set, Tomsk, Not set
Not set, Barcelona, Not set
Not set, Barcelona, Not set
Not set, Madrid, Not set
Not set, Valencia, Not set
Not set, Birmingham, Not set
Not set, London, Not set
Not set, Manchester, Not set
Not set, Plymouth, Not set
Not set, Sutton, Not set
Not set, Yeovil, Not set
Conditions: Ovarian Cancer
301 - 312 of 344
