Science and Research

Pharmacokinetic and Pharmacodynamic Modelling to Characterize the Tolerability of Alternative Up-Titration Regimens of Roflumilast in Patients with Chronic Obstructive Pulmonary Disease

BACKGROUND: In the OPTIMIZE study, 4 weeks of roflumilast 250 microg once daily before escalation to the approved 500 microg once daily maintenance dose reduced treatment discontinuations and improved tolerability to roflumilast among patients with chronic obstructive pulmonary disease (COPD). In this study, we present the pharmacokinetic (PK) results and PK/pharmacodynamic (PD) modelling data from OPTIMIZE. METHODS: OPTIMIZE was a multicentre, double-blind, phase III study in which patients with severe COPD were randomized 1:1:1 to receive oral roflumilast 250 mug once daily, 500 mug every other day, or 500 mug once daily for 4 weeks, followed by 500 mug once daily for 8 weeks. A population PK (popPK) model characterized roflumilast exposure levels (total phosphodiesterase-4 inhibition [tPDE4i]). Furthermore, models characterized the percentage of patients with adverse events (AEs) of interest (PK/AE model), and time to discontinuation due to such AEs (PK/time-to-event model). RESULTS: The popPK model adequately described average plasma concentrations and variability from 1238 patients. The percentage of patients with AEs of interest increased with predicted tPDE4i exposure (logit scale slope 0.484; confidence interval 0.262-0.706; p = 2 x 10(-5)). PK/time-to-event model analysis predicted that patients receiving the 250 mug up-titration regimen had significantly lower discontinuation rates and longer time to discontinuation compared with roflumilast 500 mug every other day or 500 mug once daily (p = 0.0014). CONCLUSIONS: In this PK/PD model, a 4-week up-titration regimen with roflumilast 250 microg once daily was found to reduce discontinuations and improve tolerability, confirming the main clinical findings of the OPTIMIZE study. However, use of this lower dose as long-term maintenance therapy may not induce sufficient phosphodiesterase-4 inhibition to exert clinical efficacy, supporting the approval of 500 microg as maintenance dose. TRIAL REGISTRATION: OPTIMIZE: NCT02165826; REACT: NCT01329029.

  • Facius, A.
  • Marostica, E.
  • Gardiner, P.
  • Watz, H.
  • Lahu, G.
Publication details
DOI: 10.1007/s40262-018-0671-4
Journal: Clinical pharmacokinetics
Pages: 1029-1038 
Number: 8
Work Type: Original
Location: ARCN
Disease Area: COPD
Partner / Member: Ghd
Access-Number: 29797235
See publication on PubMed

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