Triheptanoin: First Approval

Drugs. 2020 Oct;80(15):1595-1600. doi: 10.1007/s40265-020-01399-5.

Abstract

Triheptanoin (Dojolvi™), a synthetic medium-chain triglyceride, is being developed by Ultragenyx Pharmaceutical as a pharmaceutical-grade anaplerotic compound for use in the treatment of inherited metabolic disorders. In June 2020, triheptanoin received its first regulatory approval, in the USA, for use as a source of calories and fatty acids for the treatment of pediatric and adult patients with molecularly confirmed long-chain fatty acid oxidation disorders (LC-FAOD). Triheptanoin has also been investigated for use as a treatment in a range of other metabolic disorders or other diseases where energy deficiency is implicated. This article summarizes the milestones in the development of triheptanoin leading to this first regulatory approval for use in the treatment of pediatric and adult patients with LC-FAOD.

Publication types

  • Review

MeSH terms

  • Animals
  • Clinical Trials, Phase II as Topic
  • Clinical Trials, Phase III as Topic
  • Disease Models, Animal
  • Drug Approval*
  • Drug Evaluation, Preclinical
  • Energy Metabolism / drug effects
  • Fatty Acids / metabolism*
  • Humans
  • Lipid Metabolism, Inborn Errors / diet therapy*
  • Lipid Metabolism, Inborn Errors / genetics
  • Lipid Metabolism, Inborn Errors / metabolism
  • Oxidation-Reduction
  • Treatment Outcome
  • Triglycerides / administration & dosage*
  • Triglycerides / adverse effects
  • United States
  • United States Food and Drug Administration / legislation & jurisprudence

Substances

  • Fatty Acids
  • Triglycerides
  • triheptanoin