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

Author:

Deal Cheri L1,Steelman Joel2,Vlachopapadopoulou Elpis3,Stawerska Renata4,Silverman Lawrence A5,Phillip Moshe6,Kim Ho-Seong7,Ko CheolWoo8,Malievskiy Oleg9,Cara Jose F10,Roland Carl L11,Taylor Carrie Turich10,Valluri Srinivas Rao10,Wajnrajch Michael P1012,Pastrak Aleksandra13,Miller Bradley S14ORCID

Affiliation:

1. Centre de recherche CHU Ste-Justine, Université de Montréal , Montréal , Canada

2. Cook Children’s Medical Center , Fort Worth, TX , USA

3. Children’s Hospital P. & A. Kyriakou , Athens , Greece

4. Polish Mother’s Memorial Hospital-Research Institute, Lodz, and Medical University of Lodz , Lodz , Poland

5. Goryeb Children’s Hospital, Atlantic Health System , Morristown, NJ , USA

6. Schneider Children’s Medical Center of Israel, Petah Tikva, and Sackler Faculty of Medicine, Tel-Aviv University , Tel-Aviv , Israel

7. Yonsei University College of Medicine , Seoul , South Korea

8. Kyungpook National University Children’s Hospital , Daegu , South Korea

9. Bashkir State Medical University , Ufa , Russia

10. Pfizer Inc , New York, NY , USA

11. Pfizer Inc , Sanford, NC , USA

12. New York University Langone Medical Center , New York, NY , USA

13. OPKO Health , Miami, FL , USA

14. University of Minnesota Masonic Children’s Hospital , Minneapolis, MN , USA

Abstract

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).

Funder

Pfizer Inc

OPKO Health

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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