Nintedanib in the management of idiopathic pulmonary fibrosis: clinical trial evidence and real-world experience

Pilar Rivera-Ortega, Conal Hayton, John Blaikley, Colm Leonard, Nazia Chaudhuri

Research output: Contribution to journalArticlepeer-review


Idiopathic pulmonary fibrosis (IPF) is a fibrotic interstitial lung disease associated with significant morbidity and mortality. Previously, IPF has been managed using immunosuppressive therapy; however, it has been shown that this is associated with increased mortality. In the last 5 years, two disease-modifying agents have been licensed for use in IPF, namely pirfenidone and nintedanib. Nintedanib is a tyrosine kinase inhibitor with antifibrotic properties that has also been shown to significantly reduce the progression of the disease. The scientific evidence shows that nintedanib is effective and well tolerated for the treatment of IPF in mild, moderate and severe stages of the disease. Real-world experiences also support the findings of previously conducted clinical trials and show that nintedanib is effective for the management of IPF and is associated with reducing disease progression. Gastrointestinal events, mainly diarrhoea, are the main adverse events caused by the treatment. Recent real-word studies also suggest that nintedanib stabilizes lung function till lung transplantation, with no increased surgical complications or postoperative mortality after lung transplantation. In this review, we will discuss the clinical trial evidence and real-world experience for nintedanib in the management of IPF.

Original languageEnglish
Number of pages13
JournalTherapeutic Advances in Respiratory Disease
Publication statusPublished - 25 Sept 2018


  • antifibrotic
  • idiopathic pulmonary fibrosis
  • interstitial lung disease
  • nintedanib


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