TABLE 1

Baseline characteristics, disease characteristics and biomarkers at VENTURE baseline

VENTURE baseline
OCS dose
≤10 mg·day−1
VENTURE baseline
OCS dose
>10 mg·day−1
Placebo/DPLDPL/DPLPlacebo/DPLDPL/DPL
Patients61603630
Age, years50.9±12.053.5±12.052.1±13.048.0±14.0
Male26 (42.6)25 (41.7)14 (38.9)12 (40.0)
Ongoing atopic or allergic condition#43 (70.5)44 (73.3)28 (77.8)21 (70.0)
Former smoker13 (21.3)16 (26.7)2 (5.6)3 (10.0)
OCS dose, mg·day−18.07 (2.06)7.42 (2.16)17.57 (5.69)18.08 (5.40)
Number of severe asthma exacerbations in the 1 year prior to parent study2.30 (2.19)1.87 (2.17)1.97 (2.52)1.97 (1.45)
Pre-bronchodilator FEV1, L1.62±0.661.50±0.481.63±0.571.58±0.55
Pre-bronchodilator FEV1, % predicted51.6±16.051.6±15.253.9±14.652.1±15.9
FEV1 reversibility, %18.6±25.222.6±26.416.9±20.720.2±20.0
ACQ-5 score, scale 0–62.54±1.142.39±1.182.69±1.062.53±1.05
AQLQ global score, scale 1–74.43±1.114.41±1.084.19±1.174.26±1.26
Blood eosinophils, cells·µL−1250 (110.0–430.0)340 (180–545.0)220 (115.0–430.00)210 (140.0–320.0)
Total IgE, IU·mL−1140.0 (36.0–494.5)185.5 (103.5–484.5)161.0 (48.0–304.5)131.0 (40.0–588.0)
FENO, ppb21.0 (15.0–44.0)28.0 (14.0–47.0)41.0 (26.0–67.0)26.0 (16.0–42.0)

Data are presented as n, mean±sd, n (%) or median (interquartile range). OCS: oral corticosteroids; DPL: dupilumab; FEV1: forced expiratory volume in 1 s; ACQ-5: five-item Asthma Control Questionnaire; AQLQ: Asthma Quality of Life Questionnaire; IgE: immunoglobulin E; FENO: fractional exhaled nitric oxide. #: a patient who has any of the following diseases: atopic dermatitis, allergic conjunctivitis or rhinitis, eosinophilic oesophagitis, food allergy or hives, or if baseline total IgE ≥100 IU·mL−1 and at least one aeroantigen-specific IgE is positive (≥0.35 IU·mL−1) at baseline.