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Study identifier: NCT05493709 Synced from ClinicalTrials.gov · August 04, 2026
● Completed

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

Condition: Puberty; Precocious, Central  ·  Sponsor: Foresee Pharmaceuticals Co., Ltd.

PhasePhase 3
Planned participants94
Who can joinAll sexes, 2 Years to 9 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (41)

Arizona UniversityTucson, Arizona, United States
Rady Children's Hospital- San DiegoSan Diego, California, United States
Nemours Children's Health CenterJacksonville, Florida, United States
Johns Hopkins - All Children's HospitalSt. Petersburg, Florida, United States
Rocky Mountain Clinical ResearchIdaho Falls, Idaho, United States
Indiana UniversityIndianapolis, Indiana, United States
University of Texas Southwestern Medical CenterDallas, Texas, United States
Cook Children'sFort Worth, Texas, United States
Virginia UniversityCharlottesville, Virginia, United States
Multicare Health SystemTacoma, Washington, United States
The Second Hospital of Anhui Medical UniversityHefei, Anhui, China
Children's Hospital affiliated to Capital Institute of PediatricsBeijing, Chaoyang District, China

+ 29 more locations — full list on the registry record.

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