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Spots Global Cancer Trial Database for Safety and Efficacy of TKI258 in FGFR1 Amplified and Non-amplified Metastatic HER2 Negative Breast Cancer

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Trial Identification

Brief Title: Safety and Efficacy of TKI258 in FGFR1 Amplified and Non-amplified Metastatic HER2 Negative Breast Cancer

Official Title: A Multi-center, Open Label Phase II Trial of TKI258 in FGFR1 Amplified and Non-amplified Metastatic or Advanced HER2 Negative Breast Cancer

Study ID: NCT00958971

Interventions

TKI258

Study Description

Brief Summary: The purpose of this trial is to determine the efficacy and safety profile of TKI258 in 3 groups of patients with metastatic HER2 negative breast cancer (BC) stratified by FGFR1 and hormone receptor (HR) status.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Comprehensive Blood and Cancer Center Dept CBCC (3), Bakersfield, California, United States

Tower Cancer Research, Beverly Hills, California, United States

UCLA/ University of California Los Angeles Div. of Hematology/Oncology, Los Angeles, California, United States

Cancer Care Associates Medical Group Dept. of CCA, Redondo Beach, California, United States

Central Coast Medical Oncology Corporation, Santa Maria, California, United States

Florida Cancer Specialists Dept.of FloridaCancerSpec. (2), Fort Myers, Florida, United States

Kansas City Cancer Center KCCC (3), Overland Park, Kansas, United States

Associates in Oncology/Hematology, P.C., Rockville, Maryland, United States

Comprehensive Cancer Centers of Nevada, Henderson, Nevada, United States

UNC/ Lineberger Comprehensive Cancer Center Dept. of Linberger Cancer Ctr, Chapel Hill, North Carolina, United States

Northwest Cancer Specialists Northwest Office (2), Portland, Oregon, United States

Texas Oncology, P.A. Dept. of Texas Oncology, Bedford, Texas, United States

Texas Oncology, P.A. Austin, Dallas, Texas, United States

Texas Oncology, P.A. Presbyterian Hospital, Dallas, Texas, United States

Texas Oncology, P.A. Texas Oncology - Sammons, Dallas, Texas, United States

Tyler Cancer Center Dept.ofTylerCancerCtr. (2), Tyler, Texas, United States

Fairfax Northern Virginia Hematology Oncology Fairfax NVH, Fairfax, Virginia, United States

Blue Ridge Research Center at Roanoke Neurological Center Blue Ridge Cancer Care, Roanoke, Virginia, United States

Novartis Investigative Site, Edmonton, Alberta, Canada

Novartis Investigative Site, Montreal, Quebec, Canada

Novartis Investigative Site, Helsinki, , Finland

Novartis Investigative Site, Lyon Cedex, , France

Novartis Investigative Site, Saint-Herblain Cédex, , France

Novartis Investigative Site, Toulouse Cedex 3, , France

Novartis Investigative Site, Villejuif Cedex, , France

Novartis Investigative Site, Cuneo, CN, Italy

Novartis Investigative Site, Cremona, CR, Italy

Novartis Investigative Site, Parma, PR, Italy

Novartis Investigative Site, Candiolo, TO, Italy

Novartis Investigative Site, Napoli, , Italy

Novartis Investigative Site, Negrar, , Italy

Novartis Investigative Site, Barcelona, Cataluña, Spain

Novartis Investigative Site, Lleida, Cataluña, Spain

Novartis Investigative Site, Madrid, , Spain

Novartis Investigative Site, Taipei, , Taiwan

Novartis Investigative Site, Glasgow, , United Kingdom

Novartis Investigative Site, London, , United Kingdom

Novartis Investigative Site, London, , United Kingdom

Contact Details

Name: Novartis Pharmaceuticals

Affiliation: Novartis Pharmaceuticals

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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