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Clinical Significance of Continuable Treatment with Nintedanib Over 12 Months for Idiopathic Pulmonary Fibrosis in a Real-World Setting.

Motoyasu KatoShinichi SasakiMisa TateyamaYuta AraiHiroaki MotomuraIssei SumiyoshiYusuke OchiJunko WatanabeHiroaki IharaShinsaku TogoKazuhisa Takahashi
Published in: Drug design, development and therapy (2021)
Poor PS can result in discontinuation of nintedanib after 12 months. Long-term nintedanib treatment may be effective for survival.
Keyphrases
  • idiopathic pulmonary fibrosis
  • interstitial lung disease
  • systemic sclerosis
  • replacement therapy