Overview

Efficacy, Safety, and Pharmacokinetics of Leuprolide Mesylate in Subjects With Central Precocious Puberty

Status:
Not yet recruiting
Trial end date:
2025-12-31
Target enrollment:
Participant gender:
Summary
The study will evaluate if Leuprolide Mesylate is safe and effective in the treatment of subjects with central (gonadotropin-dependent) precocious puberty, when administered as two injections six months apart.
Phase:
Phase 3
Details
Lead Sponsor:
Foresee Pharmaceuticals Co., Ltd.
Collaborators:
GeneScience Pharmaceuticals Co., Ltd.
QPS
Treatments:
Leuprolide