drugset / Trial / NCT02427958

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

NCT02427958

Phase 4 Completed 307 enrolled Takeda
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess long-term safety and efficacy of leuprorelin in the treatment of Central Precocious Puberty (CPP).

Timeline

Start
2015-08-07
Primary completion
2018-11-23
Completion
2018-11-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Leuprolide Other / unclassified 1.88 mg Subcutaneous
Subject Leuprolide Other / unclassified 3.75 mg Subcutaneous