Last updated on May 2020

A Study to Evaluate Safety Efficacy Pharmacokinetics and Pharmacodynamics of Leuprolide Acetate 45mg 6-Month Formulation in Children With Central Precocious Puberty (CPP)

Brief description of study

The primary objective of the study is to assess the safety and efficacy of a leuprolide acetate (LA) 45 mg 6-month depot formulation for the treatment of CPP in children who are either nave to treatment with a gonadotropin-releasing hormone agonist (GnRHa) or who have been previously treated with a GnRHa.

Clinical Study Identifier: NCT03695237

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Pediatric Endocrine Associates /ID# 201089

Greenwood Village, CO United States
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Indiana University /ID# 200526

Indianapolis, IN United States
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