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1 designed to neutralize IL-5 (mepolizumab and reslizumab).
2 esis of asthma (eg, omalizumab, mepolizumab, reslizumab).
3 d trial of the humanized anti-IL-5 antibody, reslizumab, (1.0 mg/kg IV) administered 3 to 7 days prio
4 d trial of the humanized anti-IL-5 antibody, reslizumab, (1.0 mg/kg IV) administered 3 to 7 days prio
5 assigned (1:1) to receive either intravenous reslizumab (3.0 mg/kg) or placebo every 4 weeks for 1 ye
8 , 67%, 64%, and 24% in the 1, 2, and 3 mg/kg reslizumab (all P < .001) and placebo groups, respective
9 ralizing monoclonal antibodies (mepolizumab, reslizumab and benralizumab) are currently available for
11 sessment scores; the differences between the reslizumab and placebo groups were not statistically sig
12 thways (IL-5R and IL-5), namely mepolizumab, reslizumab, and benralizumab, are effective and safe for
15 dy 1; 119 [51%] for placebo and 67 [29%] for reslizumab for study 2), upper respiratory tract infecti
21 e aimed to assess the efficacy and safety of reslizumab in patients with inadequately controlled, mod
22 toms (127 [52%] for placebo and 97 [40%] for reslizumab in study 1; 119 [51%] for placebo and 67 [29%
26 953 were randomly assigned to receive either reslizumab (n=477 [245 in study 1 and 232 in study 2]) o
27 nt received a specific volume of study drug (reslizumab or matching placebo) on the basis of the pati
32 The monoclonal antibodies mepolizumab and reslizumab target the ligand IL-5, preventing its intera
33 of treatment of the response to intravenous reslizumab treatment at 52 weeks, but it was not suitabl
36 New anti-IL-5 therapeutics, mepolizumab and reslizumab, were US Food and Drug Administration approve