Apr 12, 2015

Nintedanib in the treatment of idiopathic pulmonary fibrosis

Therapeutic Advances in Respiratory Disease
Mariano E MazzeiHarold R Collard


Idiopathic pulmonary fibrosis (IPF) is a progressive and ultimately fatal lung disease that occurs in older adults. The clinical course of IPF is variable and hard to predict in an individual patient. Nintedanib is a tyrosine kinase inhibitor that has recently been approved in the US and European Union for the treatment of IPF. Preclinical studies have shown that nintedanib interferes with processes active in fibrosis such as fibroblast proliferation, migration and differentiation and the secretion of extracellular matrix. The safety and efficacy of nintedanib have been investigated in the phase II TOMORROW trial and in two replicate 52-week randomized, placebo-controlled phase III trials known as the INPULSIS trials. These trials demonstrated that nintedanib slowed disease progression by reducing the annual rate of decline in forced vital capacity, with a manageable side-effect profile. In this review, we summarize key data supporting nintedanib as a treatment for patients with IPF and address key questions regarding the use of nintedanib in the clinical setting.

  • References24
  • Citations16


Mentioned in this Paper

Extracellular Matrix
Vital Capacity Test
Adverse Effects
Process of Secretion
Cell Differentiation Process
Protein-tyrosine kinase inhibitor
Idiopathic Pulmonary Fibrosis
Preclinical Study
Lung Diseases

Related Feeds

Cell Migration

Cell migration is involved in a variety of physiological and pathological processes such as embryonic development, cancer metastasis, blood vessel formation and remoulding, tissue regeneration, immune surveillance and inflammation. Here is the latest research.

© 2020 Meta ULC. All rights reserved