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Brief Title: Aromasin® As Adjuvant Treatment In Postmenopausal Women With Invasive, Estrogen Receptor Positive Early Breast Cancer
Official Title: A Non-Interventional Study With Aromasin® As Adjuvant Treatment In Postmenopausal Women With Invasive, Estrogen Receptor Positive Early Breast Cancer Who Are Disease-Free After 2-3 Years Of Initial Adjuvant Tamoxifen Therapy
Study ID: NCT01239745
Brief Summary: This non-interventional study will be conducted in several Eastern European countries to assess the safety, tolerability and efficacy of Aromasin® when it is administered in real-word setting in postmenopausal women with invasive estrogen receptor positive early breast cancer , who are disease-free after completion of 2 to 3 years of tamoxifen and continue the treatment with Aromasin® until completion of 5 years of adjuvant hormonal therapy, to understand how Aromasin® is used in routine clinical practice, to assess adherence to prescribed Aromasin® treatment and to understand reasons for its early discontinuation.
Detailed Description: The study prematurely discontinued on October 11, 2011 due to slow enrollment. It should be noted that safety concerns have not been seen in this study and have not factored into this decision.
Minimum Age:
Eligible Ages: CHILD, ADULT, OLDER_ADULT
Sex: FEMALE
Healthy Volunteers: No
General Hospital Karlovac, Karlovac, , Croatia
University Hospital Center Osijek, Osijek, , Croatia
General Hospital Pula, Pula, , Croatia
University Hospital Center Rijeka, Rijeka, , Croatia
University Hospital Center Split, Split, , Croatia
General Hospital Varazdin, Varazdin, , Croatia
Clinic for Tumors, Zagreb, , Croatia
University Hospital Center "Sestre milosrdnice", Zagreb, , Croatia
North Estonia Medical Centre Foundation, Tallinn, , Estonia
Institute for Oncology and Radiology of Serbia, Belgrade, , Serbia
Oncology Clinic, Medical center, Bezanijska Kosa, Beograd, , Serbia
Name: Pfizer CT.gov Call Center
Affiliation: Pfizer
Role: STUDY_DIRECTOR