Overview

Extension Study of 1.0mg Dose Letrozole Therapy in Postmenopausal Patients With Breast Cancer

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
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 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Novartis Pharmaceuticals
Collaborator:
Chugai Pharmaceutical
Treatments:
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.