Evidence map›Paper›PMID 41394116›Full record

ArticleJournal of the Endocrine Society2026

Seven-year Safety and Efficacy of Somapacitan in Children With GH Deficiency: Final Results From REAL 3.

Lars Sävendahl, Tadej Battelino, Michael Højby, Tina Leunbach, Paul Saenger, Lawrence Silverman, Reiko Horikawa

Registry-linked trialAbstract read
In one paragraph

Article in Journal of the Endocrine Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02616562 (A Randomised, Multinational, Active-controlled,), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02616562 phase2completednot on this map

A Randomised, Multinational, Active-controlled, (Open-labelled), Dose Finding, (Double-blinded), Parallel Group Trial Investigating Efficacy and Safety of Once-weekly NNC0195-0092 Treatment Compared to Daily Growth Hormone Treatment (Norditropin® FlexPro®) in Growth Hormone Treatment naïve Pre-pubertal Children With Growth Hormone Deficiency

TypeinterventionalSponsorNovo Nordisk A/SRan2016 to 2024Enrolled76ConditionsGrowth Hormone Disorder, Growth Hormone Deficiency in ChildrenArmssomapacitan, Norditropin® FlexPro® pen
3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Lars SävendahlPediatric Endocrinology, Karolinska University Hospital and Department of Women's and Children's Health, Karolinska Institutet, Solna 171 77, Sweden.ORCID https://orcid.org/0000-0003-1067-4976
Tadej BattelinoFaculty of Medicine, University of Ljubljana, and University Medical Center Ljubljana, Ljubljana 1000, Slovenia.ORCID https://orcid.org/0000-0002-0273-4732
Michael HøjbyClinical Drug Development, Novo Nordisk A/S, Søborg 2860, Denmark.
Tina LeunbachClinical Drug Development, Novo Nordisk A/S, Søborg 2860, Denmark.
Paul SaengerPediatric Endocrinology, NYU Langone Health, Mineola, NY 11501, USA.
Lawrence SilvermanPediatric Endocrinology, Goryeb Children's Hospital, Atlantic Health, Morristown, NJ 07962, USA.
Reiko HorikawaDivision of Endocrinology and Metabolism, National Center for Child Health and Development, Tokyo 157-8535, Japan.ORCID https://orcid.org/0000-0003-3429-3246

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Somapacitan is a once-weekly GH treatment that has shown efficacy and safety profiles equivalent to daily GH in children with GH deficiency (GHD). Objective: To investigate long-term safety, efficacy, and treatment burden associated with somapacitan after 7 years (364 weeks) of treatment. Methods: REAL 3 (NCT02616562) was a phase 2, randomized, open-label trial investigating the efficacy and safety of somapacitan vs daily GH in children with GHD. After 156 weeks, participants entered a 208-week safety extension. Children in cohort I (age 2.5-10.0 years) previously completed 3 years in the trial; cohort II (age <2.5 years) and cohort III (age 9.0-17.0 years) entered the trial at week 156 for safety-only assessment. All participants received somapacitan 0.16 mg/kg/week. Height velocity (HV), HV SD score (SDS), height SDS, IGF-I SDS, incidence of adverse events (AEs), and treatment burden were assessed. Results: Overall, 43 participants (73%) in cohort I, 1 participant (100%) in cohort II, and 11 participants (69%) in cohort III completed the 208-week safety extension. Consistent increments in HV and HV SDS were seen in cohort I, and height SDSs at week 364 were close to 0. The incidence of AEs was aligned with previous investigations across all cohorts; 3 serious AEs in cohort I were considered probably/possibly related to treatment. Treatment burden was reduced in children who switched from daily GH to somapacitan. Conclusion: After 7 years of treatment, children with GHD receiving somapacitan experienced consistent increases in height SDS and reduced treatment burden. No new safety concerns were identified.

Indexed as

childhood growth hormone deficiencygrowth hormone treatmentlong-acting growth hormonesomapacitan

Identifiers

PMID41394116
PMCPMC12699150

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.