# Two-year real-world experience with somatrogon in children and adolescents with growth hormone deficiency

**Authors:** Gianluca Tamaro, Chiara Rodaro, Alice Fachin, Antonella Fabretto, Gianluca Tornese

PMC · DOI: 10.3389/fendo.2026.1685851 · Frontiers in Endocrinology · 2026-01-28

## TL;DR

A study of children and teens with growth hormone deficiency found that weekly somatrogon treatment was safe and effective, though growth gains were lower than in clinical trials.

## Contribution

This is the first real-world study of somatrogon in pediatric GHD patients over two years, showing practical benefits and growth outcomes.

## Key findings

- Height SDS increased significantly at 6 months in both new and switched patients.
- Naïve patients showed greater height gains at 18 and 24 months compared to switch patients.
- Treatment was well tolerated with no discontinuations and improved adherence reported.

## Abstract

Growth hormone deficiency (GHD) in children and adolescents is a chronic condition requiring long-term therapy with recombinant human growth hormone (rhGH). Daily injections pose adherence challenges, prompting the development of long-acting GH (LAGH) formulations, such as once-weekly somatrogon. While phase III trials have demonstrated its efficacy, real-world data are limited.

This retrospective study evaluated all pediatric patients with GHD who initiated somatrogon between March 2023 and January 2025 at a tertiary endocrine center in Italy and completed at least 6 months of treatment.

Forty patients (50% naïve; 50% switched from daily rhGH) were included. At 6 months, height SDS increased significantly in both naïve (Δ +0.19) and switch patients (Δ +0.17), with no significant difference between groups. However, by 18 and 24 months, naïve patients showed significantly greater height gains, with a median cumulative Δ of +0.81 at 18 months. IGF-1 SDS increased significantly only in the naïve group. Median gain in height SDS at 12 months in naïve patients (+0.37) was lower than reported in registration trials, likely reflecting the broader clinical heterogeneity of real-world populations. Treatment was well tolerated, with no discontinuations and few mild adverse events. Several families reported improved adherence and quality of life.

In this first real-world cohort, somatrogon was safe and effective in supporting linear growth, although height gains were lower than in clinical trials. Weekly administration may offer practical benefits, especially for patients with complex needs or poor adherence to daily injections.

## Full-text entities

- **Genes:** GH1 (growth hormone 1) [NCBI Gene 2688] {aka GH, GH-N, GHB5, GHN, IGHD1A, IGHD1B}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, GGH (gamma-glutamyl hydrolase) [NCBI Gene 8836] {aka GATD10, GH}
- **Diseases:** GHD (MESH:D004393)
- **Chemicals:** somatrogon (MESH:C000723339)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12890668/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12890668/full.md

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Source: https://tomesphere.com/paper/PMC12890668