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

PHASE3CompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

February 29, 2016

Primary Completion Date

May 31, 2017

Study Completion Date

December 19, 2017

Conditions
Prostatic Neoplasms
Interventions
DRUG

LMIS 50 mg

Subcutaneous injection of 50 mg Leuprolide Mesylate

Trial Locations (7)

28025

Carolina Clinical Trials, LLC, Concord

29572

Carolina Urologic Research Center, Myrtle Beach

35209

Urology Centers of Alabama, Homewood

83642

Idaho Urologic Institute - Meridian, Meridian

92123

Genesis Research, LLC, San Diego

98166

Seattle Urology Research Center, Burien

08648

AdvanceMed Research, Lawrenceville

All Listed Sponsors
collaborator

QPS-Qualitix

INDUSTRY

lead

Foresee Pharmaceuticals Co., Ltd.

INDUSTRY