drugset / Trial / NCT07710430

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

NCT07710430

Phase 4 Not yet recruiting 43 enrolled LG Chem
NaSingle-groupOpen-labelTreatment

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

Timeline

Start
2026-08-01
Primary completion
2029-08-30
Completion
2030-04-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Leuprolide Other / unclassified