Phase I-II Study to Determine the Maximum Tolerated Dose (MTD) of AUY922 in Advanced Solid Malignancies, and Efficacy in HER2+ or ER+ Locally Advanced or Metastatic Breast Cancer Patients

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

117

Participants

Timeline

Start Date

July 31, 2007

Primary Completion Date

April 30, 2012

Study Completion Date

April 30, 2012

Conditions
Breast CancerHematologic Neoplasms
Interventions
DRUG

AUY922 2 mg/m2

Trial Locations (10)

6500

Novartis Investigative Site, Bellinzona

30912

Georgia Health Sciences University Med College of GA, Augusta

63110

Washington University School Of Medicine-Siteman Cancer Ctr Dept. of Siteman Cancer Ctr., St Louis

78229

Cancer Therapy & Research Center / UT Health Science Center InstituteForDrugDevelopment(3), San Antonio

89135

Nevada Cancer Institute Clinical Trials Office, Las Vegas

90095

UCLA/ University of California Los Angeles UCLA, Los Angeles

02115

Dana Farber Cancer Institute StudyCoordinator:CAUY922A2101, Boston

77030-4009

MD Anderson Cancer Center/University of Texas Thoractic Head/Neck Med.Onc(2), Houston

9713 GZ

Novartis Investigative Site, Groningen

SM2 5PT

Novartis Investigative Site, Sutton

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY