A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension

Trial Profile

A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension

Recruiting
Phase of Trial: Phase II

Latest Information Update: 06 Aug 2017

At a glance

  • Drugs Bardoxolone methyl (Primary)
  • Indications Idiopathic pulmonary fibrosis; Pneumonia; Pulmonary arterial hypertension; Sarcoidosis
  • Focus Therapeutic Use
  • Acronyms LARIAT
  • Sponsors Reata Pharmaceuticals
  • Most Recent Events

    • 24 May 2017 Results of an interim analysis from expanded connective tissue disease patients (n=22) presented at the 113th International Conference of the American Thoracic Society
    • 14 Nov 2016 According to a Reata Pharmaceuticals Media Release, based on the data of an analysis assessing risk factors and its risk mitigation strategy for managing acute fluid retention from BEACON trial, FDA approved the Phase 2 program in PAH (LARIAT). Data from CATALYST and LARIAT trials will be utilized for a New Drug Application review of the safety profile of the drug.
    • 13 Oct 2016 Planned End Date changed from 1 Dec 2016 to 1 Sep 2018.
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