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Table 2 Demographic characteristics

From: Exposure–safety analyses of nintedanib in patients with chronic fibrosing interstitial lung disease

Characteristic

TOMORROW (IPF)

n = 342a

INPULSIS-1 (IPF)

n = 513

INPULSIS-2 (IPF)

n = 548

SENSCIS (SSc-ILD)

n = 576

INBUILD (Progressive fibrosing ILD)

n = 663

Age, years

65 (8.4)

67 (8.3)

67 (7.8)

54 (12.2)

66 (9.8)

Body weight, kg

77 (14.7)

82 (16.6)

77 (16.1)

70 (15.9)

77 (17.4)

Height, cm

167 (9.0)

169 (8.9)

167 (9.4)

164 (9.8)

165 (10.0)

FVC, % predicted

82 (17.9)

80 (17.1)

79 (18.4)

73 (16.7)

69 (15.6)

Race, n (%)

 White

270 (79)

333 (65)

275 (50)

387 (67)

488 (74)

 Black

0

0

2 (< 1)

36 (6)

10 (2)

 Asian

72 (21)

106 (21)

214 (39)

143 (25)

163 (25)

 American Indian/Alaska native

0

1 (< 1)

1 (< 1)

5 (1)

0

 Hawaiian/Pacific Islander

0

0

0

1 (< 1)

1 (< 1)

 Multiple

0

0

0

4 (< 1)

1 (< 1)

 Missing

0

73 (14)b

56 (10)b

0

0

Region, n (%)

 Asia

73 (21)

97 (19)

225 (41)

130 (23)

155 (23)

 Europe

202 (59)

288 (56)

187 (34)

266 (46)

301 (45)

 North America

10 (3)

70 (14)

104 (19)

142 (25)

136 (21)

 Rest of the world

57 (17)

58 (11)

32 (6)

38 (7)

71 (11)

Underlying diagnosis (INBUILD STUDY), n (%)

 HP

173 (26)

 iNSiP

125 (19)

 Unclassifiable IIP

114 (17)

 Autoimmune ILDs

170 (26)

 Other ILDs

81 (12)

  1. Data are presented as mean (SD) unless otherwise stated
  2. FVC forced vital capacity, HP hypersensitivity pneumonitis, IIP idiopathic interstitial pneumonia, ILD interstitial lung disease, iNSiP idiopathic nonspecific interstitial pneumonia, IPF idiopathic pulmonary fibrosis, SD standard deviation, SSc systemic sclerosis
  3. aFrom 428 patients treated in the TOMORROW trial, 342 patients are shown (86 patients randomized to 50 mg nintedanib once daily were excluded from analysis)
  4. bDue to local laws, race information was not collected for some patients with study site located in France