Table 1.

Baseline characteristics for patients in the PEGASUS study with and without hemolysis events

Patients with hemolysis event (n = 19)Patients without hemolysis event (n = 61)
Age, y   
Mean (range) 54.5 (28-78) 47.0 (19-81) 
>65, n (%) 7 (37) 10 (16) 
Sex, n (%)   
Female 7 (37) 42 (69) 
Body mass index, mean (SD), kg/m2 27.5 (4.5) 26.0 (4.2) 
No transfusions in previous 12 mo, n (%) 4 (21) 16 (26) 
≥4 transfusions in previous 12 mo, n (%) 13 (68) 31 (51) 
History of thrombosis, n (%) 8 (42) 17 (28) 
On-label eculizumab dose at screening (900 mg every 2 wk), n (%) 9 (47) 47 (77) 
Higher-than-label eculizumab dose at screening (>900 mg every 2 wk), n (%) 10 (53) 14 (23) 
1200 mg every 2 wk  9 (47) 13 (21) 
1500 mg every 2 wks 1 (5) 1 (2) 
Hb, mean (SD), g/dL 8.8 (1.0) 8.6 (1.0) 
LDH, mean (SD), U/L 305.6 (212.6) 275.2 (211.7) 
Complement CH50, mean (SD), U/mL 19.7 (27.6) 5.4 (16.0) 
Detectable complement CH50, n (%) 14 (74) 33 (54) 
Patients with hemolysis event (n = 19)Patients without hemolysis event (n = 61)
Age, y   
Mean (range) 54.5 (28-78) 47.0 (19-81) 
>65, n (%) 7 (37) 10 (16) 
Sex, n (%)   
Female 7 (37) 42 (69) 
Body mass index, mean (SD), kg/m2 27.5 (4.5) 26.0 (4.2) 
No transfusions in previous 12 mo, n (%) 4 (21) 16 (26) 
≥4 transfusions in previous 12 mo, n (%) 13 (68) 31 (51) 
History of thrombosis, n (%) 8 (42) 17 (28) 
On-label eculizumab dose at screening (900 mg every 2 wk), n (%) 9 (47) 47 (77) 
Higher-than-label eculizumab dose at screening (>900 mg every 2 wk), n (%) 10 (53) 14 (23) 
1200 mg every 2 wk  9 (47) 13 (21) 
1500 mg every 2 wks 1 (5) 1 (2) 
Hb, mean (SD), g/dL 8.8 (1.0) 8.6 (1.0) 
LDH, mean (SD), U/L 305.6 (212.6) 275.2 (211.7) 
Complement CH50, mean (SD), U/mL 19.7 (27.6) 5.4 (16.0) 
Detectable complement CH50, n (%) 14 (74) 33 (54) 

CH50, total complement function; Hb, hemoglobin; LDH, lactate dehydrogenase; SD, standard deviation.

One patient in the pegcetacoplan group received 900 mg of eculizumab every 11 days.

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