A Study to Assess the Efficacy and Safety of the Triptorelin 6-month Formulation in Paediatric Participants With Central Precocious Puberty.

PHASE3CompletedINTERVENTIONAL
Enrollment

66

Participants

Timeline

Start Date

August 10, 2021

Primary Completion Date

August 21, 2022

Study Completion Date

February 13, 2023

Conditions
Central Precocious Puberty
Interventions
DRUG

Triptorelin Pamoate

Triptorelin 6-month formulation for IM on day 1 and Month 6.

Trial Locations (14)

100045

Beijing Children's Hospital, Capital Medical University, Beijing

130021

No.1 Hospital of Jilin University (Bethune first hospital of Jilin University), Changchun

201102

Children's Hospital of Fudan University, Changhai

214023

Wuxi children's Hospital, Wuxi

215031

Children's Hospital of Soochow University, Suzhou

250021

Shandong Provincial Hospital, Jinan

276016

Linyi Maternal and Child Health Care Hospital, Linyi

330006

Jiangxi Provincial Children's Hospital, Nanchang

337000

Pingxiang Maternity and Child Care, Pingxiang

410007

Hunan children's hospital, Changsha

430015

Wuhan Children's Hospital Tongji Medical College Huazhong University of Science & Technology, Wuhan

430030

Tongji Hospital, Tongji Medical College, Huazhong University of Science & Technology, Wuhan

450018

Zhengzhou Children's Hospital , Henan Children's Hospital, Zhengzhou

610073

Chengdu Women's & Children's Central Hospital, Chengdu

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Ipsen

INDUSTRY

NCT05029622 - A Study to Assess the Efficacy and Safety of the Triptorelin 6-month Formulation in Paediatric Participants With Central Precocious Puberty. | Biotech Hunter | Biotech Hunter