drugset / Trial / NCT02427958
A Study to Assess the Safety and Efficacy of Leuprorelin in Central Precocious Puberty in Chinese Participants
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Leuprolide | Other / unclassified | 1.88 mg | Subcutaneous |
| Subject | Leuprolide | Other / unclassified | 3.75 mg | Subcutaneous |