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Clinical Trial Summary

This study evaluates the safety and efficiency of Pegylated Somatropin (PEG Somatropin) Injection in the treatment of endogenous growth hormone deficiency (GHD) in the broad population of children. Half of participants will receive the high dose, while the other half will receive the low dose.


Clinical Trial Description

n/a


Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02314676
Study type Interventional
Source GeneScience Pharmaceuticals Co., Ltd.
Contact Junfen Fu, Ph.D
Phone 13777457849
Email fjf68@qq.com
Status Recruiting
Phase Phase 4
Start date November 2014

See also
  Status Clinical Trial Phase
Completed NCT01187550 - Predictive Markers in Chinese Growth Hormone Deficiency (GHD) Children Treated With Saizen® Phase 4
Completed NCT00102258 - Role of Nutrition and Hormones in Boys With Disordered Growth Phase 2
Completed NCT00097513 - National Cooperative Growth Study (NCGS) of Optimal Nutropin AQ and Nutropin Dosing in Pubertal Growth Hormone-Deficient (GHD) Patients Phase 4
Completed NCT00097526 - Bone Mineral Density (BMD) in Adolescents With Growth Hormone Deficiency (GHD) Phase 4