Developments in the Management of Growth Hormone Deficiency: Clinical Utility of Somapacitan.

(3–6): growth hormone adherence adult growth hormone deficiency long-acting growth hormone pediatric growth hormone deficiency

Journal

Drug design, development and therapy
ISSN: 1177-8881
Titre abrégé: Drug Des Devel Ther
Pays: New Zealand
ID NLM: 101475745

Informations de publication

Date de publication:
2024
Historique:
received: 12 10 2023
accepted: 11 01 2024
medline: 9 2 2024
pubmed: 9 2 2024
entrez: 9 2 2024
Statut: epublish

Résumé

Growth hormone (GH) replacement therapy for growth hormone deficiency (GHD) in children and adults has for over 25 years, until recently, been administered as daily injections. This daily treatment regimen often incurs a burden to patients and caregivers, leading to high rates of non-adherence and, consequently, decreased treatment efficacy outcomes. To address this shortcoming, long-acting growth hormones (LAGHs) have been developed with the aim of reducing the burden of daily injections, thereby potentially improving treatment adherence and outcomes. Somapacitan (Sogroya

Identifiants

pubmed: 38333899
doi: 10.2147/DDDT.S315172
pii: 315172
pmc: PMC10849900
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

291-306

Informations de copyright

© 2024 Miller et al.

Déclaration de conflit d'intérêts

B.S.M.: Consulted for Ascendis Pharma, BioMarin, Bristol Myers Squibb, EMD Serono, Endo Pharmaceuticals, Eton Pharmaceuticals, GenSci, Novo Nordisk, Orchard Therapeutics, Pfizer, Provention Bio, and Tolmar; and received research support from Alexion, AbbVie, Ascendis Pharma, Aeterna Zentaris, Amgen, Amicus, Foresee Pharmaceuticals, Lumos Pharma, Lysogene, Novo Nordisk, OPKO Health, Pfizer, Prevail Therapeutics, and Sangamo Therapeutics. J.B.: Received honoraria for presentations at meetings sponsored by Novo Nordisk, Sandoz, and Ipsen; received sponsorship to attend scientific meetings from Novo Nordisk; and received payment for membership of the Publication Steering Committee of the International Outcomes Study, sponsored by Novo Nordisk. R.H: Advisory board member and lecturer for Novo Nordisk, Pfizer, Lumos Pharma, JCR, and Sandoz. A.L.: Consulted for/received research funding/honoraria from Novo Nordisk, Merck Serono, Alexion, AstraZeneca Rare Disease, and Pfizer Inc; and received honoraria from Ipsen and Sandoz. K.C.J.Y.: Received research grants to Barrow Neurological Institute from Crinetics, Ascendis, Corcept, Amryt, and Sparrow; served as an occasional advisory board member for Novo Nordisk, Ascendis, Ipsen, Amryt, Crinetics, Recordati, Neurocrine, and Xeris; lecture fees from Pfizer; and served as occasional speaker for Recordati and Novo Nordisk.

Auteurs

Bradley S Miller (BS)

Division of Pediatric Endocrinology, University of Minnesota Medical School, MHealth Fairview Masonic Children's Hospital, Minneapolis, MN, USA.

Jo Blair (J)

Department of Paediatric Endocrinology, Alder Hey Children's NHS Foundation Trust, Liverpool, UK.

Reiko Horikawa (R)

Division of Endocrinology and Metabolism, National Center for Child Health and Development, Tokyo, Japan.

Agnès Linglart (A)

Department of Endocrinology and Diabetes for Children, Hospital Bicêtr Paris Saclay, AP-HP, Le Kremlin-Bicêtre, France.
Unité 1185, INSERM, Paris, France.
Reference Center for Rare Pituitary Disorders, Hospital Bicêtre Paris Saclay, AP-HP, Le Kremlin-Bicêtre, France.
Platform of Expertise for Rare Diseases, OSCAR Network, Hospital Bicêtre Paris Saclay, AP-HP, Le Kremlin-Bicêtre, France.

Kevin C J Yuen (KCJ)

Departments of Neuroendocrinology and Neurosurgery, Barrow Neurological Institute, University of Arizona College of Medicine and Creighton School of Medicine, Phoenix, AZ, USA.

Classifications MeSH