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: TakedaTreatments: Leuprolide