Survodutide in MASH: bridging the gap between hepatic and systemic metabolic dysfunction


Kaya E., YILMAZ Y., Alkhouri N.

Expert Opinion on Investigational Drugs, cilt.33, sa.12, ss.1167-1176, 2024 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Derleme
  • Cilt numarası: 33 Sayı: 12
  • Basım Tarihi: 2024
  • Doi Numarası: 10.1080/13543784.2024.2441865
  • Dergi Adı: Expert Opinion on Investigational Drugs
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1167-1176
  • Anahtar Kelimeler: diabetes, fibrosis, metabolic disorders, comorbidities, metabolic dysfunction-associated steatohepatitis, Metabolic dysfunction-associated steatotic liver disease, obesity, survodutide
  • Recep Tayyip Erdoğan Üniversitesi Adresli: Evet

Özet

Introduction: Glucagon-like peptide-1 receptor (GLP-1 R) agonists have demonstrated remarkable effectiveness in the treatment of obesity and type 2 diabetes. Although these agents provide beneficial effects for metabolic dysfunction-associated steatohepatitis (MASH) through their glucose-lowering and weight-reducing properties, their efficacy in promoting fibrosis regression remains unproven. Survodutide, an investigational dual agonist that simultaneously targets both the glucagon receptor (GCGR) and GLP-1 R, has emerged as a promising therapeutic candidate for the comprehensive management of obesity and MASH. By engaging these two critical receptors, this drug has the potential to offer a broad spectrum of metabolic benefits, addressing multiple pathogenic mechanisms underlying these interrelated disorders. Areas covered: This review examines the pharmacological profile, clinical efficacy, and safety data of survodutide derived from phase 1 and 2 clinical trials. Expert opinion: Survodutide’s dual agonism of the GCGR and GLP-1 R may surpass the efficacy of selective GLP-1 R agonists, demonstrating significant potential in resolving MASH and promoting fibrosis regression. The drug is generally well tolerated, with primarily manageable gastrointestinal adverse effects. As survodutide progresses through phase 3 clinical development, its potential to provide a more effective and holistic approach to treating MASH and its comorbidities may significantly improve patient outcomes and quality of life.