Study identifier:D8664L00012
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Protection of Ovarian Function with Goserelin Acetate in Premenopausal Early Breast Cancer Patients Undergoing Adjuvant Chemotherapy: An Open Label, Randomised, Multi-Centre, Phase IIIb Study
Breast Cancer
Phase 3
No
Goserelin acetate
Female
102
Interventional
18 Years - 45 Years
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Prevention
Verified 01 Dec 2010 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
-
No locations available
Arms | Assigned Interventions |
---|---|
No Intervention: A Patients receiving only adjuvant chemotherapy | - |
Experimental: B Patient receiving goserelin acetate along with adjuvant chemotherapy | Drug: Goserelin acetate 3.6 mg depot injectable preparation Other Name: Zoladex 3.6 mg Depot |