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Safety, Tolerability and Efficacy of TransCon hGH Weekly Versus Daily hGH in Chinese Pediatric Growth Hormone Deficiency

Growth Hormone Deficiency Clinical Trial

Official title:
The Efficacy, Safety and Tolerability of TransCon hGH Administered Weekly Versus Daily hGH in Prepubertal Children With Growth Hormone Deficiency: a Randomized, Open-lable, Active-controlled, Parallel-group Study in China

Clinical Trial Summary

This study is conducted in China only. The purpose is to demonstrate the efficacy and safety of once weekly dosing of TransCon hGH, a long-acting growth hormone product, compare to once-daily dosing of human growth hormone (hGH) after 52 weeks of treatment in prepubertal children with growth hormone deficiency (GHD).

Clinical Trial Description

Not Provided ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04326374
Study type Interventional
Source Visen Pharmaceuticals (Shanghai) Co., Ltd.
Contact Lisa Chen, MD
Phone +86-02152999605
Email lisa.chen@visenpharma.com
Status Recruiting
Phase Phase 3
Start date December 30, 2019
Completion date April 2022
View Details
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