Clinical trial

Safety, Efficacy, and Pharmacokinetic Behavior of Leuprolide Mesylate in…

NCT02234115 · Foresee Pharmaceuticals Co., Ltd., Industry · Completed

Key facts

NCT number NCT02234115
Title Safety, Efficacy, and Pharmacokinetic Behavior of Leuprolide Mesylate in Subjects With Advanced Prostate Carcinoma
Official title An Open-Labeled, Singled-Arm Study of the Safety, Efficacy, and Pharmacokinetic Behavior of Leuprolide Mesylate for Injectable Suspension (LMIS 50 mg) in Subjects With Advanced Prostate Carcinoma
Lead sponsor Foresee Pharmaceuticals Co., Ltd., Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Prostatic Neoplasms
Intervention type Drug
Interventions Leuprolide Mesylate
Enrollment 137
Start date Aug 1, 2014
Primary completion Aug 30, 2016
Completion Jan 5, 2017
First posted Sep 9, 2014
Last update posted Mar 5, 2019
Countries Austria, Czechia, Germany, Lithuania, Poland, Slovakia, Taiwan, United States

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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