Overview

Open-Label Safety Extension Study in Patients Who Have Previously Participated and Have Benefited From LMIS 50 mg

Status:
Completed
Trial end date:
2017-12-19
Target enrollment:
Participant gender:
Summary
This is a safety extension of up to 12 months of additional treatment with LMIS 50 mg after the subject has completed 12 months of treatment under Protocol FP01C-13-001 and remain eligible for continued treatment with androgen deprivation therapy. Subjects participating in Protocol FP01C-13-001-EX will be followed for safety only.
Phase:
Phase 3
Details
Lead Sponsor:
Foresee Pharmaceuticals Co., Ltd.
Collaborator:
QPS-Qualitix
Treatments:
Leuprolide