Table 3.

Other secondary efficacy outcomes at day 183

Ravulizumab (n = 96)Eculizumab (n = 95)
Total number of packed red blood cell units transfused, mean (SD) — 4.3 (4.76) — 3.4 (3.01) 
Patients with major adverse vascular events, n (%) — 0 (0) — 0 (0) 
Ravulizumab (n = 96)Eculizumab (n = 95)
Total number of packed red blood cell units transfused, mean (SD) — 4.3 (4.76) — 3.4 (3.01) 
Patients with major adverse vascular events, n (%) — 0 (0) — 0 (0) 
Baseline*Day 183Baseline*Day 183
Clinical manifestations of PNH, n (%)     
 Fatigue 29 (30.2) 42 (43.8) 38 (40) 36 (37.9) 
 Abdominal pain 5 (5.2) 5 (5.2) 6 (6.3) 12 (12.6) 
 Dyspnea 6 (6.3) 6 (6.3) 10 (10.5) 17 (17.9) 
 Dysphagia 2 (2.1) 5 (5.2) 2 (2.1) 5 (5.2) 
 Chest pain 0 (0) 2 (2.1) 1 (1.1) 5 (5.2) 
 Hemoglobinuria 4 (4.2) 8 (8.3) 7 (7.4) 9 (9.5) 
 Erectile dysfunction§ 5 (10.0) 6 (12.0) 7 (14.6) 6 (12.5) 
Baseline*Day 183Baseline*Day 183
Clinical manifestations of PNH, n (%)     
 Fatigue 29 (30.2) 42 (43.8) 38 (40) 36 (37.9) 
 Abdominal pain 5 (5.2) 5 (5.2) 6 (6.3) 12 (12.6) 
 Dyspnea 6 (6.3) 6 (6.3) 10 (10.5) 17 (17.9) 
 Dysphagia 2 (2.1) 5 (5.2) 2 (2.1) 5 (5.2) 
 Chest pain 0 (0) 2 (2.1) 1 (1.1) 5 (5.2) 
 Hemoglobinuria 4 (4.2) 8 (8.3) 7 (7.4) 9 (9.5) 
 Erectile dysfunction§ 5 (10.0) 6 (12.0) 7 (14.6) 6 (12.5) 
*

Baseline was defined as the last nonmissing value before the first dose of study drug.

n = 97.

n = 98.

§

n = 50 male patients in the ravulizumab group and n = 48 male patients in the eculizumab group.

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