Somatrogon: First Approval

Drugs. 2022 Feb;82(2):227-234. doi: 10.1007/s40265-021-01663-2.

Abstract

Somatrogon (NGENLA®), a long-acting human growth hormone based on C-terminal peptide technology, is in development by Pfizer and OPKO Health for the treatment of growth hormone deficiency in pediatric and adult patients. Administered as a once-weekly subcutaneous injection, somatrogon reduces treatment burden relative to once-daily human growth hormone therapy while providing non-inferior efficacy. Somatrogon received its first approval in October 2021 in Canada for the long-term treatment of pediatric patients who have growth failure due to an inadequate secretion of endogenous growth hormone (growth hormone deficiency). This article summarizes the milestones in the development of somatrogon leading to this first approval for the treatment of growth hormone deficiency.

Publication types

  • Review

MeSH terms

  • Canada
  • Clinical Trials, Phase II as Topic
  • Clinical Trials, Phase III as Topic
  • Drug Approval
  • Drug Interactions
  • Human Growth Hormone* / deficiency
  • Humans
  • Multicenter Studies as Topic

Substances

  • Human Growth Hormone
  • somatrogon