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An Open Label Study to Determine the Safety and Tolerability of 12 Weeks Treatment With Oral REN001 in Subjects With Fatty Acid Oxidation Disorders (FAOD)

Trial Profile

An Open Label Study to Determine the Safety and Tolerability of 12 Weeks Treatment With Oral REN001 in Subjects With Fatty Acid Oxidation Disorders (FAOD)

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 13 Dec 2022

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At a glance

  • Drugs Mavodelpar (Primary)
  • Indications Metabolic disorders
  • Focus Adverse reactions
  • Sponsors Reneo Pharmaceuticals

Most Recent Events

  • 07 Dec 2022 Status changed from active, no longer recruiting to completed.
  • 09 Aug 2022 According to a Reneo Pharmaceuticals media release, data from this trial will be presented at the International Network for Fatty Acid Oxidation Research and Management (INFORM) Conference, Aug 28-29 (Freiburg, Germany).
  • 26 Jul 2022 Results published in Reneo Pharmaceuticals Media Release.

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