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. 2018 Sep 21;9:321–328. doi: 10.2147/PROM.S144425

Table 1.

Comparison of antifibrotic agents approved for the treatment of IPF

Nintedanib Pirfenidone
Efficacy • Slower rate of decline in forced vital capacity over 1 year when compared with placebo
• Reduction in acute exacerbations
• Lower all-cause mortality at 1 year
• Slower rate of decline in forced vital capacity over 1 year when compared with placebo
• Improved progression-free survival
• Reduction in respiratory-related hospitalizations
• Lower all-cause mortality at 1 year
Potential side effects • Diarrhea
• Weight loss
• Elevated liver enzymes
• Nausea
• Photosensitivity
• Elevated liver enzymes
Dosing • One capsule taken twice per day • Three capsules taken three times per day
Contraindications • No absolute contraindications
• Not recommended in Child Pugh Class B or C hepatic impairment
• Caution in patients with high cardiovascular risk or high risk for bleeding
• No absolute contraindications
Impact on quality of life • Slower rate of decline in respiratory-specific quality of life as measured by St. George’s Respiratory Questionnaire • May slow the progression of worsening dyspnea

Abbreviation: IPF, idiopathic pulmonary fibrosis.