Pegylated Somatropin (PEG Somatropin) in the Treatment of Children With Growth Hormone Deficiency

NCT03249480 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 900

Last updated 2017-08-15

No results posted yet for this study

Summary

To Evaluate the safety and efficacy of PEG Somatropin in the treatment of children with growth hormone deficiency, as well as to study the dosage of PEG Somatropin.

Conditions

  • Growth Hormone Deficiency

Interventions

BIOLOGICAL

PEG-somatropin

30IU/10 mg/3ml/kit, 0.1-0.2mg /kg/w, once per day for 26 weeks.

Sponsors & Collaborators

  • Beijing Children's Hospital

    collaborator OTHER
  • Tianjin Medical University General Hospital

    collaborator OTHER
  • Peking University Third Hospital

    collaborator OTHER
  • China-Japan Friendship Hospital

    collaborator OTHER
  • Dalian Children's Hospital

    collaborator OTHER
  • Xian Children's Hospital

    collaborator OTHER_GOV
  • Wuhan Children's Hospital

    collaborator OTHER
  • Fuzhou Children s Hospital

    collaborator UNKNOWN
  • Anhui Provincial Children's Hospital

    collaborator OTHER
  • Hunan Children's Hospital

    collaborator OTHER_GOV
  • Shenzhen Children's Hospital

    collaborator OTHER_GOV
  • Children's Hospital of Hebei Province

    collaborator OTHER
  • Second Affiliated Hospital of Xi'an Jiaotong University

    collaborator OTHER
  • Zhengzhou Children's Hospital, China

    collaborator OTHER
  • Children's Hospital of Soochow University

    collaborator OTHER
  • Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region

    collaborator OTHER
  • First Affiliated Hospital of Kunming Medical University

    collaborator OTHER
  • Kunming Children's Hospital

    collaborator OTHER
  • The First People's Hospital of Yunnan

    collaborator OTHER
  • Xuzhou Children's Hopspital

    collaborator UNKNOWN
  • Henan Provincial People's Hospital

    collaborator OTHER
  • The First Affiliated Hospital of Henan University of Traditional Chinese Medicine

    collaborator OTHER
  • First Affiliated Hospital of Harbin Medical University

    collaborator OTHER
  • The Second Hospital of Hebei Medical University

    collaborator OTHER
  • Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

    collaborator OTHER
  • Union Hospital of Tongji Medical College of HUST

    collaborator UNKNOWN
  • Wuxi Women's & Children's Hospital

    collaborator OTHER
  • The Second Affiliated Hospital of Kunming Medical University

    collaborator OTHER
  • Nanjing Children's Hospital

    collaborator OTHER
  • Changchun GeneScience Pharmaceutical Co., Ltd.

    lead INDUSTRY

Principal Investigators

  • Chunxiu Gong · Beijing Children's Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
3 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2017-08-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03249480 on ClinicalTrials.gov