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No relevant pharmacokinetic drug-drug interaction between nintedanib and pirfenidone.
Richeldi, Luca; Fletcher, Sophie; Adamali, Huzaifa; Chaudhuri, Nazia; Wiebe, Sabrina; Wind, Sven; Hohl, Kathrin; Baker, Andrew; Schlenker-Herceg, Rozsa; Stowasser, Susanne; Maher, Toby M.
Affiliation
  • Richeldi L; Università Cattolica del Sacro Cuore, Fondazione Policlinico A. Gemelli, Rome, Italy.
  • Fletcher S; Dept of Respiratory Medicine, University Hospital Southampton and Southampton NIHR Respiratory Biomedical Research Unit, University Hospital Southampton, Southampton, UK.
  • Adamali H; Dept of Respiratory Medicine, University Hospital Southampton and Southampton NIHR Respiratory Biomedical Research Unit, University Hospital Southampton, Southampton, UK.
  • Chaudhuri N; Translational Research Collaboration - Inflammatory Respiratory Disease Centre, Manchester, UK.
  • Wiebe S; Bristol Interstitial Lung Disease Service, North Bristol NHS Trust, Southmead Hospital, Bristol, UK.
  • Wind S; Translational Research Collaboration - Inflammatory Respiratory Disease Centre, Manchester, UK.
  • Hohl K; North West Lung Centre, Manchester University NHS Foundation Trust, Manchester, UK.
  • Baker A; Boehringer Ingelheim Pharma, Biberach, Germany.
  • Schlenker-Herceg R; Boehringer Ingelheim Pharma, Biberach, Germany.
  • Stowasser S; Boehringer Ingelheim Pharma, Biberach, Germany.
  • Maher TM; Boehringer Ingelheim, Bracknell, UK.
Eur Respir J ; 53(1)2019 01.
Article in En | MEDLINE | ID: mdl-30442716
Nintedanib and pirfenidone are approved treatments for idiopathic pulmonary fibrosis (IPF). This open-label, two-group trial investigated the pharmacokinetic drug-drug interaction between these two drugs in patients with IPF.Subjects not treated with antifibrotics at screening (group 1, n=20) received a single nintedanib dose (150 mg) followed by pirfenidone (titrated to 801 mg thrice daily) for 3 weeks, with a further single nintedanib dose (150 mg) on the last day (day 23). Subjects treated with pirfenidone at screening (group 2, n=17) continued to receive pirfenidone alone (801 mg thrice daily) for 7 days, then co-administered with nintedanib (150 mg twice daily) for a further 7 days, before single doses of both treatments on day 16.In group 1, adjusted geometric mean (gMean) ratios (with/without pirfenidone) were 88.6% and 80.6% for nintedanib area under the plasma concentration-time curve (AUC) and maximum plasma concentration (Cmax), respectively. In group 2, gMean ratios (with/without nintedanib) were 97.2% and 99.5% for pirfenidone AUC and Cmax, respectively. For all parameters, the 90% confidence intervals included 100%, suggesting similar exposure for administration alone and when co-administered. Both treatments were well tolerated.These data indicate there is no relevant pharmacokinetic drug-drug interaction between nintedanib and pirfenidone when co-administered in IPF patients.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyridones / Idiopathic Pulmonary Fibrosis / Indoles Type of study: Clinical_trials Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Eur Respir J Year: 2019 Type: Article Affiliation country: Italy

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyridones / Idiopathic Pulmonary Fibrosis / Indoles Type of study: Clinical_trials Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Eur Respir J Year: 2019 Type: Article Affiliation country: Italy