BENITIONSClinical Trial Intelligence

A Study of Leuprolide Acetate Depot in Children With Central Precocious Puberty

4期 已完成 NCT05341115

适应症Central Precocious Puberty
分期4期
申办方Takeda
状态已完成
受试者人数79 人
干预(药物)Leuprorelin Acetate Depot 3M
开始日期2023年3月12日
完成日期2024年12月19日
结果公布日2026年1月13日

摘要

The main aim is to see how leuprolide works to treat central precocious puberty in children. Participants will receive an injection of leuprorelin acetate depot 11.25 mg every 12 weeks during 6 months and will visit their study clinic 6 times to complete some assessments.

Percentage of Participants With Peak Luteinizing Hormone (LH) Suppression in Gonadotropin-Releasing Hormone (GnRH) Stimulation at Week 24

Week 24 · percentage of participants

Leuprorelin Acetate Depot 3M 11.25 mg96.20 percentage of participants

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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。