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Table 1 Baseline demographics and spirometry (safety set)

From: A blinded evaluation of the efficacy and safety of glycopyrronium, a once-daily long-acting muscarinic antagonist, versus tiotropium, in patients with COPD: the GLOW5 study

 

Glycopyrronium 50 μg o.d. (N = 327)

Tiotropium 18 μg o.d. (N = 330)

Mean (SD) age, years

63.2 (7.9)

63.7 (8.0)

Male, n (%)

237 (72.5)

248 (75.2)

Ethnicity, n (%)

  

   Caucasian

225 (68.8)

232 (70.3)

   Black

0

0

   Asian

95 (29.1)

91 (27.6)

   Native American

6 (1.8)

7 (2.1)

   Other

1 (0.3)

0

Severity of COPD (GOLD 2010), n (%)

  

   Mild

0

1 (0.3)

   Moderate

191 (58.4)

193 (58.5)

   Severe

136 (41.6)

136 (41.2)

Mean (SD) duration of COPD, years

6.5 (5.1)

6.2 (5.1)

Baseline COPD exacerbation history*, n (%)

  

   0 exacerbations

255 (78.0)

247 (74.8)

   1 exacerbation

52 (15.9)

61 (18.5)

   ≥2 exacerbations

20 (6.1)

22 (6.7)

ICS use at baseline, n (%)

163 (49.8)

174 (52.7)

Smoking history, n (%)

  

   Ex-smoker

179 (54.7)

182 (55.2)

   Current smoker

148 (45.3)

148 (44.8)

Mean (SD) duration of smoking, pack-years

39.6 (20.4)

40.2 (21.5)

Mean (SD) FEV1 post-bronchodilator, L

1.5 (0.5)

1.5 (0.5)

Mean (SD) post-bronchodilator FEV1% predicted

53.2 (13.1)

53.9 (12.7)

Mean (SD) post-bronchodilator FEV1 reversibility, %

17.9 (13.5)

17.6 (13.6)

Mean (SD) post-bronchodilator FEV1/FVC, %

47.4 (10.7)

47.2 (10.5)

  1. Pack-years = total years of smoking multiplied by cigarette packs smoked per day; *In the year prior to screening; FEV1 = forced expiratory volume in 1 second; FVC = forced vital capacity; SD = standard deviation; o.d. = once-daily.