Continued Treatment with Nintedanib in Patients with Progressive Pulmonary Fibrosis: Data from INBUILD-ON

Lung. 2025 Jan 9;203(1):25. doi: 10.1007/s00408-024-00778-z.

Abstract

Purpose: In the INBUILD trial in patients with progressive pulmonary fibrosis (PPF), nintedanib slowed the decline in forced vital capacity (FVC) versus placebo, with a safety profile characterised mainly by gastrointestinal events. INBUILD-ON, the open-label extension of INBUILD, assessed the safety of nintedanib during longer-term treatment. Data on FVC were collected.

Study design and methods: Adverse events and changes in FVC in INBUILD-ON were assessed descriptively in all patients and in two subgroups: patients who received nintedanib in INBUILD and continued nintedanib in INBUILD-ON ("continued nintedanib" group) (n = 212) and patients who received placebo in INBUILD and initiated nintedanib in INBUILD-ON ("initiated nintedanib" group) (n = 222). Changes in FVC were based on observed values.

Results: Median exposure to nintedanib in INBUILD-ON was 22.0 months. Diarrhoea was the most frequent adverse event. Amongst patients who had diarrhoea, 90.0% experienced only events of mild or moderate severity. Adverse events led to discontinuation of nintedanib at a rate of 16.7 per 100 patient-years. Serious and fatal adverse events were reported at rates of 37.2 and 9.5 per 100 patient-years. Mean (SE) changes in FVC from baseline to week 48 were - 71.6 (16.1) mL [- 128.5 (25.5) mL in continued nintedanib group (n = 106), - 14.8 (18.2) mL in initiated nintedanib group (n = 106)].

Conclusion: The safety profile of nintedanib in INBUILD-ON was consistent with that in INBUILD. Change in FVC in INBUILD-ON was consistent with decline in FVC in the nintedanib group of INBUILD. These results support the use of nintedanib in the long-term treatment of PPF.

Clinical trial registration: ClinicalTrials.gov; NCT03820726; registered January 29, 2019.

Keywords: Clinical trial; Drug tolerance; Interstitial lung disease; Pulmonary function tests; Vital capacity.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Aged
  • Antifibrotic Agents / adverse effects
  • Antifibrotic Agents / therapeutic use
  • Diarrhea* / chemically induced
  • Disease Progression*
  • Female
  • Humans
  • Idiopathic Pulmonary Fibrosis / drug therapy
  • Idiopathic Pulmonary Fibrosis / physiopathology
  • Indoles* / administration & dosage
  • Indoles* / adverse effects
  • Indoles* / therapeutic use
  • Lung / drug effects
  • Lung / physiopathology
  • Male
  • Middle Aged
  • Protein Kinase Inhibitors / administration & dosage
  • Protein Kinase Inhibitors / adverse effects
  • Protein Kinase Inhibitors / therapeutic use
  • Pulmonary Fibrosis / drug therapy
  • Pulmonary Fibrosis / physiopathology
  • Time Factors
  • Treatment Outcome
  • Vital Capacity

Substances

  • nintedanib
  • Indoles
  • Protein Kinase Inhibitors
  • Antifibrotic Agents

Associated data

  • ClinicalTrials.gov/NCT03820726