Breast Cancer Clinical Trial

Trial Evaluating Dovitinib Combined With Fulvestrant, in Postmenopausal Patients With HER2- and HR+ Breast Cancer

Summary

This trial is designed to enroll postmenopausal patients with locally advanced or metastatic, HER2- and HR+ breast cancer not amenable to curative treatment by surgery or radiotherapy, and whose disease has progressed on or after prior endocrine therapy.

Patients must undergo molecular pre-screening prior to entry.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Postmenopausal women with HER2-, HR+ locally advanced or metastatic breast cancer
Progression on or after endocrine treatment
Measureable disease as per RECIST
ECOG 0, 1 or 2

Exclusion Criteria:

Evidence of CNS or leptomeningeal metastases
Previous treatment with fulvestrant
Previous chemotherapy for locally advanced or metastatic breast cancer
Cirrhosis or chronic active/persistent hepatitis

Other protocol-defined inclusion/exclusion criteria may apply

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

97

Study ID:

NCT01528345

Recruitment Status:

Terminated

Sponsor:

Novartis Pharmaceuticals

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There are 67 Locations for this study

See Locations Near You

Ironwood Cancer and Research Centers SC
Chandler Arizona, 85224, United States
Highlands Oncology Group Dept of Highlands Oncology Grp
Fayetteville Arkansas, 72703, United States
City of Hope National Medical Center COH 3
Duarte California, 91010, United States
University of California San Diego - Moores Cancer Center Moores UCSD Cancer Ctr. SC-1
La Jolla California, 92093, United States
Cedars Sinai Medical Center Samuel Oschin Cancer Center
Los Angeles California, 90048, United States
H. Lee Moffitt Cancer Center & Research Institute H. Lee Moffitt SC
Tampa Florida, 33612, United States
Oncology Specialists, SC Lutheran General Advanced Care
Park Ridge Illinois, 60068, United States
Indiana University Health Goshen Center for Cancer SC
Goshen Indiana, 46526, United States
Nebraska Methodist Hospital Estabrook Cancer Center
Omaha Nebraska, 68114, United States
Saint Barnabas Medical Center CancerCenter of Saint Barnabas
Livingston New Jersey, 07039, United States
ProHealth Care
Lake Success New York, 11042, United States
New York Oncology Hematology, P.C. Dept. of New York Oncology. PC
Troy New York, 12180, United States
Duke University Medical Center Duke (SC)
Durham North Carolina, 27710, United States
Cancer Centers of the Carolinas Dept. of CC of the Carolinas
Greenville South Carolina, 29605, United States
Cancer Care Centers of South Texas / HOAST CCC of So. TX- San Antonio(2)
San Antonio Texas, 78229, United States
Virginia Cancer Specialists, PC Dept.ofFairfax SC
Fairfax Virginia, 22031, United States
Medical Oncology Associates, PS
Spokane Washington, 99208, United States
Wenatchee Valley Medical Center Wenatchee Valley
Wenatchee Washington, 98801, United States
Novartis Investigative Site
Rio Negro Viedma, 8500, Argentina
Novartis Investigative Site
Buenos Aires , C1050, Argentina
Novartis Investigative Site
Cordoba , X5006, Argentina
Novartis Investigative Site
Tucuman , T4000, Argentina
Novartis Investigative Site
Salzburg , 5020, Austria
Novartis Investigative Site
Wien , 1090, Austria
Novartis Investigative Site
Leuven , 3000, Belgium
Novartis Investigative Site
Wilrijk , 2610, Belgium
Novartis Investigative Site
Salvador BA, 40170, Brazil
Novartis Investigative Site
Londrina PR, 86015, Brazil
Novartis Investigative Site
Porto Alegre RS, 90610, Brazil
Novartis Investigative Site
Sao Jose do Rio Preto SP, 15090, Brazil
Novartis Investigative Site
São Paulo SP, 01317, Brazil
Novartis Investigative Site
Besançon cedex , 25030, France
Novartis Investigative Site
Bordeaux , 33076, France
Novartis Investigative Site
Lille Cedex , 59020, France
Novartis Investigative Site
Saint-Herblain Cédex , 44805, France
Novartis Investigative Site
Thonon-les-Bains Cedex , 74203, France
Novartis Investigative Site
Villejuif Cedex , 94805, France
Novartis Investigative Site
Budapest , 1134, Hungary
Novartis Investigative Site
Budapest , 1145, Hungary
Novartis Investigative Site
Budapest , H-108, Hungary
Novartis Investigative Site
Debrecen , 4032, Hungary
Novartis Investigative Site
Gyor , H-902, Hungary
Novartis Investigative Site
Szeged , H-672, Hungary
Novartis Investigative Site
Szolnok , H-500, Hungary
Novartis Investigative Site
Macerata MC, 62100, Italy
Novartis Investigative Site
Parma PR, 43100, Italy
Novartis Investigative Site
Sondrio SO, 23100, Italy
Novartis Investigative Site
Maastricht , 6229 , Netherlands
Novartis Investigative Site
Rotterdam , 3075 , Netherlands
Novartis Investigative Site
Surquillo Lima, 34, Peru
Novartis Investigative Site
Poznan , 60-56, Poland
Novartis Investigative Site
Rzeszow , 35-02, Poland
Novartis Investigative Site
Warszawa , 02-78, Poland
Novartis Investigative Site
Warszawa , 03-29, Poland
Novartis Investigative Site
Warszawa , 04-12, Poland
Novartis Investigative Site
Ryazan Russia, 39001, Russian Federation
Novartis Investigative Site
St. Petersburg , 19775, Russian Federation
Novartis Investigative Site
Cape Town , 7500, South Africa
Novartis Investigative Site
Parktown , 2193, South Africa
Novartis Investigative Site
Port Elizabeth , 6045, South Africa
Novartis Investigative Site
Toledo Castilla la Mancha, 45071, Spain
Novartis Investigative Site
Barcelona Catalunya, 08035, Spain
Novartis Investigative Site
Valencia Comunidad Valenciana, 46010, Spain
Novartis Investigative Site
Madrid , 28007, Spain
Novartis Investigative Site
Niaosong Township , 83301, Taiwan
Novartis Investigative Site
Taichung , 407, Taiwan
Novartis Investigative Site
Taipei , 10048, Taiwan

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

97

Study ID:

NCT01528345

Recruitment Status:

Terminated

Sponsor:


Novartis Pharmaceuticals

How clear is this clinincal trial information?

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