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Efficacy and Safety of Weekly Somatrogon vs Daily Somatropin in Children With Growth Hormone Deficiency: A Phase 3 Study

Authors
 Cheri L Deal  ;  Joel Steelman  ;  Elpis Vlachopapadopoulou  ;  Renata Stawerska  ;  Lawrence A Silverman  ;  Moshe Phillip  ;  Ho-Seong Kim  ;  CheolWoo Ko  ;  Oleg Malievskiy  ;  Jose F Cara  ;  Carl L Roland  ;  Carrie Turich Taylor  ;  Srinivas Rao Valluri  ;  Michael P Wajnrajch  ;  Aleksandra Pastrak  ;  Bradley S Miller 
Citation
 JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, Vol.107(7) : e2717-e2728, 2022-07 
Journal Title
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
ISSN
 0021-972X 
Issue Date
2022-07
MeSH
Body Height ; Child ; Child, Preschool ; Dwarfism, Pituitary* / drug therapy ; Female ; Growth Disorders / drug therapy ; Growth Hormone / therapeutic use ; Human Growth Hormone* / adverse effects ; Humans ; Male ; Recombinant Proteins / adverse effects
Keywords
growth hormone ; growth hormone deficiency ; long-acting growth hormone ; pediatric ; somatrogon ; somatropin
Abstract
Context: Somatrogon is a long-acting recombinant human growth hormone (rhGH) in development for once-weekly treatment of children with growth hormone deficiency (GHD).

Objective: We aimed to compare the efficacy and safety of once-weekly somatrogon with once-daily somatropin in prepubertal children with GHD.

Methods: In this 12-month, open-label, randomized, active-controlled, parallel-group, phase 3 study, participants were randomized 1:1 to receive once-weekly somatrogon (0.66 mg/kg/week) or once-daily somatropin (0.24 mg/kg/week) for 12 months. A total of 228 prepubertal children (boys aged 3-11 years, girls aged 3-10 years) with GHD, impaired height and height velocity (HV), and no prior rhGH treatment were randomized and 224 received ≥1 dose of study treatment (somatrogon: 109; somatropin: 115). The primary endpoint was annualized HV at month 12.

Results: HV at month 12 was 10.10 cm/year for somatrogon-treated subjects and 9.78 cm/year for somatropin-treated subjects, with a treatment difference (somatrogon-somatropin) of 0.33 (95% CI: -0.24, 0.89). The lower bound of the 2-sided 95% CI was higher than the prespecified noninferiority margin (-1.8 cm/year), demonstrating noninferiority of once-weekly somatrogon vs daily somatropin. HV at month 6 and change in height standard deviation score at months 6 and 12 were similar between both treatment groups. Both treatments were well tolerated, with a similar percentage of subjects experiencing mild to moderate treatment-emergent adverse events in both groups (somatrogon: 78.9%, somatropin: 79.1%).

Conclusion: The efficacy of once-weekly somatrogon was noninferior to once-daily somatropin, with similar safety and tolerability profiles. (ClinicalTrials.gov no. NCT02968004).
Files in This Item:
T202205305.pdf Download
DOI
10.1210/clinem/dgac220
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pediatrics (소아과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Ho Seong(김호성) ORCID logo https://orcid.org/0000-0003-1135-099X
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/191619
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