Clinical Trials · NCT05110170

Efficacy and Safety of LY01005 in Patients With Breast Cancer Compared to ZOLADEX®

CompletedPhase 3Gonadorelin (Approved)
Phase
Phase 3
Recruitment status
Completed
Sponsor
Luye Pharma Group Ltd.
Enrollment
188
Start date
Oct 2020
Locations
1 site, China
Primary endpoint
Non-inferiority of LY01005 compared with ZOLADEX®: the percentage of subjects with serum E2 maintaining at postmenopausal level (≤30 pg/mL) from Week 4 to Week 12 after the first dose.
View Gonadorelin compound reference