Table 1.

Concizumab dose escalation during the main + extension parts of explorer4 (HAwI, HBwI) and explorer5 (HA) according to hemophilia subtype; full analysis set

Dose escalation*HA (n = 36)HAwI (n = 15)HBwI (n = 10)
None, 0.15 mg /kg only 15 (41.7) 7 (46.7) 5 (50.0) 
One, 0.15 and 0.20 mg/kg 10 (27.8) 6 (40.0) 3 (30.0) 
Two, 0.15, 0.20, and 0.25 mg/kg 11 (30.6) 2 (13.3) 2 (20.0) 
Dose escalation*HA (n = 36)HAwI (n = 15)HBwI (n = 10)
None, 0.15 mg /kg only 15 (41.7) 7 (46.7) 5 (50.0) 
One, 0.15 and 0.20 mg/kg 10 (27.8) 6 (40.0) 3 (30.0) 
Two, 0.15, 0.20, and 0.25 mg/kg 11 (30.6) 2 (13.3) 2 (20.0) 
*

Data are presented as n (percentage of patients) with dose escalation.

One HA patient with 2 escalations was later de-escalated to concizumab 0.15 mg/kg, and one HA patient with 2 escalations was later de-escalated to concizumab 0.20 mg/kg before a further escalation to concizumab 0.25 mg/kg.

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