Overview
Extension Study of 1.0mg Dose Letrozole Therapy in Postmenopausal Patients With Breast Cancer
Status:
Completed
Completed
Trial end date:
1969-12-31
1969-12-31
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
- To investigate the safety of letrozole monotherapy at a dose 1.0 mg/day or fadrozole monotherapy at a dose 2.0mg in Japanese postmenopausal patients with advanced breast cancer which participated in double blind study.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Novartis PharmaceuticalsCollaborator:
Chugai PharmaceuticalTreatments:
Letrozole
Criteria
Inclusion Criteria:- Patients which participated in double blind study
Exclusion Criteria:
- Patients with intolerable toxicity.
- Patients which confirmed progressive disease during double blind study.
- Patients which have received concurrent anti-cancer therapy during double blind study.