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. 2023 Oct 2;9(5):00249-2023. doi: 10.1183/23120541.00249-2023

TABLE 2.

Primary end-point: time to sustained clinical response

Overall Period 2 only#
Tozorakimab+SoC
(n=53)
SoC
(n=44)
Tozorakimab+SoC
(n=49)
SoC
(n=32)
Patients with a sustained clinical response 42 (79.2) 32 (72.7) 39 (79.6) 22 (68.8)
Censored 11 (20.8) 12 (27.3) 10 (20.4) 10 (31.3)
Time to response, days 8.0 (5.0–22.0) 9.5 (4.0–NE) 8.0 (5.0–22.0) 8.5 (54.5–NE)
HR (80% CI); p-value 0.96 (0.70–1.31); 0.33 1.09 (0.77–1.54)

Data are presented as n (%) or median (interquartile range), unless otherwise stated. SoC: standard of care; NE: not estimable. #: data for period 1 were not analysed separately owing to the very small proportion of patients recruited in period 1.