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P275 Comparing clinically relevant improvement with umeclidinium/vilanterol and tiotropium/olodaterol in symptomatic copd: a randomised non-inferiority crossover trial
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  1. C Compton1,
  2. G Feldman2,
  3. AR Sousa3,
  4. D Lipson4,
  5. I Naya5,
  6. L Tombs6,
  7. S Patel1,
  8. B Alcázar Navarrete7
  1. 1Global Respiratory Franchise, GSK, Brentford, UK
  2. 2South Carolina Pharmaceutical Research, Spartanburg, US
  3. 3Discovery Medicine, GSK, Uxbridge, UK
  4. 4Respiratory Research and Development, GSK, King of Prussia, US
  5. 5Respiratory Medicine, GSK, Brentford, UK
  6. 6GSK, Uxbridge, UK
  7. 7Neumología, Hospital de Alta Resolución de Loja, Granada, Spain

Abstract

Introduction and Objectives Here we report the Results of the first direct comparison of the once-daily fixed-dose long-acting muscarinic antagonist/long-acting β2-agonist (LAMA/LABA) combinations umeclidinium/vilanterol (UMEC/VI) 62.5/25 mcg and tiotropium/olodaterol (TIO/OLO) 5/5 mcg in patients with chronic obstructive pulmonary disease (COPD).

Methods This randomised, 2-period crossover study (204990, NCT02799784) included inhaled corticosteroid-free patients with COPD, a modified Medical Research Council dyspnoea score ≥2, forced expiratory volume in 1 s (FEV1)/forced vital capacity ratio of <0.70 and post-salbutamol FEV150%–70% predicted. Patients were randomised to UMEC/VI (62.5/25 mcg once daily) via an ELLIPTA dry powder inhaler followed by TIO/OLO 5/5 mcg (2 puffs once daily) via a RESPIMAT inhaler (each for 8 weeks with an interim 3 week washout period), or vice versa. The primary endpoint was change from baseline (CFB) in trough FEV1 at Week 8 with a non-inferiority (NI) margin of –50 mL in the per protocol (PP) population. Additional outcomes included inspiratory capacity (IC), rescue medication use and ease of inhaler use (assessed using a six-point questionnaire). Adverse events (AEs) were also assessed.

Results 236 patients (mean age 64.4 years, 60% male) were included in the intent-to-treat (ITT) population and 227 in the PP population. The primary endpoint of CFB in trough FEV1 at Week 8 confirmed NI of UMEC/VI vs TIO/OLO (175 mL vs 122 mL; least squares mean difference 53 mL [95% confidence interval: 26, 80]; p<0.001; PP population) and demonstrated superiority in the ITT population (Table). Patients receiving UMEC/VI were significantly more likely to achieve clinically meaningful improvements (≥100 mL) in trough FEV1 at Weeks 4 and 8 vs TIO/OLO, and showed significant improvements at Weeks 4 and 8 in IC and rescue medication use (Table). The ELLIPTA inhaler was rated higher than RESPIMAT in all ease-of-use questionnaire items (p≤0.001). The incidence of on-treatment AEs was similar in both groups (UMEC/VI, n=59 [25%]; TIO/OLO, n=71 [31%]).

Conclusions In this first, direct, once-daily LAMA/LABA comparison, a greater likelihood of improvements in lung function was demonstrated with UMEC/VI vs TIO/OLO. The ELLIPTA inhaler was preferred to RESPIMAT. Both LAMA/LABAs were well tolerated.

Funding GSK (204990 [NCT02799784])

Please refer to page A261 for declarations of interest in relation to abstract P275.

Abstract P275 Table 1

Summary of changes from baseline in lung function endpoints and rescue medication use, and trough FEV1 responder analysis (ITT population)

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