Overview

A Study to Assess the Safety and Efficacy of Leuprorelin in Central Precocious Puberty in Chinese Participants

Status:
Completed
Trial end date:
2018-11-23
Target enrollment:
Participant gender:
Summary
The purpose of this study is to assess long-term safety and efficacy of leuprorelin in the treatment of Central Precocious Puberty (CPP).
Phase:
Phase 4
Details
Lead Sponsor:
Takeda
Treatments:
Leuprolide