PiaSky® is available for C5i-naïve and C5i-experienced patients, with consistent efficacy and safety among both patient populations
*Patients starting PiaSky® will receive an initial weight-based loading dose through IV infusion, administered by their healthcare provider. Four subsequent loading doses are then given weekly by subcutaneous injection. Weight-based maintenance dosing is then administered once every 4 weeks subcutaneously. Patients may self-inject after receiving training from their healthcare provider.2
†Patients were assessed after 17 weeks of crovalimab, patients randomized to eculizumab who switched to PiaSky® in the extension period (n=38), only patients with available data (having completed the questionnaire) were included in the calculations of percentages. Questionnaire completion rate was 83%.8
‡Treatment preference among patients in COMMODORE 1 and 2 who were randomized to receive eculizumab (arm B) and switched to PiaSky® in the extension period.
§In COMMODORE 1, a non-randomized arm including patients previously treated with ravulizumab was not included in the randomized arm, patients were assessed after 17 weeks of crovalimab, patients who switched from ravulizumab to PiaSky® (n=15), only patients with available data (having completed the questionnaire) were included in the calculations of percentages. Questionnaire completion rate was 88%.9
¶PiaSky® treatment begins with a single IV weight-based loading dose administered in the clinic.
C5 = complement protein 5; IV=intravenous; IVH = intravascular hemolysis; PNH = paroxysmal nocturnal hemoglobinuria; SC = subcutaneous; SNP = single nucleotide polymorphism; TICR = transient immune complex reactions; wt = wildtype.