Kamenitz, 21204, Serbia
NCT Number: NCT02443467
A Study to Determine the Safety and Tolerability of Herceptin as an Adjuvant Therapy of Early Breast Cancer
This was an open-labeled, multi-center, prospective, non-comparative study of the safety of Herceptin (trastuzumab) used as an adjuvant therapy in patients with early breast cancer who had previously received antracycline therapy before or after surgery.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
Female
Study type
Observational
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Female patients > or = 18 years of age
- Human Epidermal Growth Factor Receptor 2 (HER2)-neu overexpression
- Previously treated with adjuvant antracycline containing chemotherapy
- Left Ventricular Ejection Fraction (LVEF) > 50%
- Eastern Cooperative Oncology Group (ECOG) score < or = 2
- Life expectancy > or = 12 weeks
Exclusion criteria
- Left Ventricular Ejection Fraction (LVEF) < 50%
- Advanced pulmonary disease
- Severe dyspnea
- Abnormal laboratory results within 14 days prior to registration
- Peripheral neuropathy
- Presence of Central Nervous System (CNS) metastasis
Treatment and study plan
No intervention
OtherPrimary outcomes
-
Percentage of participants with adverse events
Time frame: Up to 3 years
-
Percentage of participants with serious adverse events
Time frame: Up to 3 years
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Lead sponsor
Hoffmann-La Roche
Industry
Registry information
Important dates
- Study start
- 2006
- Primary completion
- 2009
- Study completion
- 2009
- First posted
- May 13, 2015
- Registry last updated
- Nov 2, 2016
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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