Clinical Trial

A Study of Leuprorelin 1-Month (4-Week) Formulation in Children With Central Precocious Puberty

Recruiting Phase 4
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Summary
A Single-Arm, Open-Label, Multicenter, Prospective Clinical Study to Evaluate the Effectiveness and Safety of Leuprorelin 1-Month (4-Week) Formulation Administered for 24 Months in Children with Central Precocious Puberty
Protocol Amendment History 1 change
critical Recruitment opened 2026-07-30
Trial Details
NCT Number NCT07710430
Lead Sponsor LG Chem
Conditions Central Precocious Puberty
Enrollment 43 participants
Start Date 2026-08-01
Primary Completion 2029-08-30 (estimated)
Study Completion 2030-04-30 (estimated)
Updated on ClinicalTrials.gov 2026-07-29