Somapacitan Treatment in Children and Adolescents Born SGA: Two-Year Efficacy and Preference Over Daily GH
Abstract Context Children born small for gestational age (SGA) without spontaneous catch-up growth may require GH treatment; however, daily injections are burdensome. Somapacitan is a once-weekly long-acting GH. Objective To assess efficacy and safety of once-weekly somapacitan in children born SGA, including outcomes after switching from daily GH. Design REAL8 is a randomized, multinational, open-label, active-controlled phase 3 study with a 52-week main period and 104-week extension (NCT05330325). REAL9 (NCT05723835) is a multinational, open-label, uncontrolled phase 3 study. Setting Clinics across Europe, Asia, and the Americas. Participants REAL8 randomized 142 GH-treatment-naïve, prepubertal children born SGA; 141 received treatment and 139 completed 104 weeks. REAL9 enrolled 12 children/adolescents born SGA (GH-naïve or previously treated). Interventions In REAL8, participants were randomized (2:1:1) to somapacitan 0.24 mg/kg/week or daily GH (0.035 or 0.067 mg/kg/day) for 52 weeks; all received 0.24 mg/kg/week somapacitan in weeks 52–104. In REAL9, participants received 0.24 mg/kg/week somapacitan for 26 weeks. Main Outcome Measures Annualized height velocity (HV); secondary outcomes included height SD score (HSDS). Results In REAL8, mean HV during weeks 52–104 remained above baseline across groups (8.5–8.8 cm/year), including after switching from daily GH; HSDS increased through week 104, and IGF-I SDS were similar between groups. In REAL9, HV increased in GH-naïve participants and was maintained in previously treated participants. Somapacitan was well-tolerated; adverse events were mostly mild and injection-site reactions were infrequent. Most participants switching from daily GH preferred somapacitan. Conclusions In children born SGA, once-weekly somapacitan maintained efficacy through 2 years, with safety comparable to daily GH, and was preferred after switching.
Authors
- Anders Krogh Lemminger (ORCID: https://orcid.org/0000-0002-7929-7147)
- Lawrence A. Silverman
- Jan Frystyk (ORCID: https://orcid.org/0000-0002-5379-0961)
- Michael Højby Rasmussen (ORCID: https://orcid.org/0000-0002-2210-0366)
- Agnès Linglart (ORCID: https://orcid.org/0000-0003-3455-002X)
- Carlos Alberto Longui (ORCID: https://orcid.org/0000-0002-6361-5235)
- Aristides K Maniatis (ORCID: https://orcid.org/0000-0002-6705-8579)
- Kenichi Kashimada (ORCID: https://orcid.org/0000-0003-2505-5932)
- Kamil Sołtysik (ORCID: https://orcid.org/0000-0002-1539-6461)
- Volker Böttcher
- Xinran Cheng
Institutions
- Inserm (FR)
- University of Southern Denmark (DK)
- Novo Nordisk (Denmark) (DK)
- Université Paris-Saclay (FR)
- Odense University Hospital (DK)
- Irmandade da Santa Casa de Misericórdia de São Paulo (BR)
- Chengdu Women's and Children's Central Hospital (CN)
- Assistance Publique – Hôpitaux de Paris (FR)
- Goryeb Children's Hospital (US)
- Novo Nordisk (United States) (US)
- Novo Nordisk (Italy) (IT)
- National Center For Child Health and Development (JP)
- Bicêtre Hospital (FR)
- Atlantic Health System (US)
Publication Details
- Journal
- The Journal of Clinical Endocrinology & Metabolism
- Published
- 2026-10-28
- DOI
- https://doi.org/10.1210/clinem/dgag430
- Primary Topic
- Growth Hormone and Insulin-like Growth Factors
- Type
- article
- Field-Weighted Citation Impact
- 0.00