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Table 4 Changes from baseline in secondary efficacy endpoints over Weeks 1–24 (intent-to-treat population)

From: Efficacy and safety of fluticasone furoate 100 μg and 200 μg once daily in the treatment of moderate-severe asthma in adults and adolescents: a 24-week randomised study

 

FF 100 μg

FF 200 μg

 

(N = 108)

(N = 111)

Percentage of rescue-free 24-hour periods (Weeks 1–24)

n

108

109

Baseline

14.3

11.5

LS mean change from baseline (SE)

21.3 (3.05)

23.1 (3.03)

Treatment difference vs. FF 100 μg (95% CI)

NA

1.8

  

(-6.7, 10.3)

Percentage of symptom-free 24-hour periods (Weeks 1–24)

n

108

109

Baseline

6.1

4.9

LS mean change from baseline (SE)

17.5 (2.80)

19.6 (2.79)

Treatment difference vs. FF 100 μg (95% CI)

NA

2.1

  

(-5.7, 9.9)

PM peak expiratory flow (L/min) (Weeks 1–24)

n

108

109

LS mean

342.7

344.0

LS mean change from baseline (SE)

5.9 (3.26)

7.2 (3.25)

Treatment difference vs. FF 100 μg (95% CI)

NA

1.3

  

(-7.8, 10.4)

AM peak expiratory flow (L/min) (Weeks 1–24)

n

108

109

LS mean

340.8

340.6

LS mean change from baseline (SE)

13.4 (3.22)

13.2 (3.20)

Treatment difference vs. FF 100 μg (95% CI)

NA

-0.2

  

(-9.2, 8.8)

  1. Note: analysis performed using ANCOVA with covariates of baseline, region, sex, age and treatment.
  2. CI = confidence interval; FF = fluticasone furoate; LS = least squares; NA = not applicable; SE = standard error.