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. 2022 Mar 4;7(6):1165–1178. doi: 10.1016/j.ekir.2022.02.021

Table 2.

Main complement inhibitors undergoing development in kidney diseases

Target in the complement cascade Mechanism of action Drug Pharmaceutical company Type of inhibitor Mode of administration Phases of drug development Potential indications in kidney diseases
C5 Inhibition of the release of C5a and C5b, and ultimately of the formation of C5b9 Eculizumab Alexion Pharma/AstraZeneca mAb i.v. Commercialized aHUS
Ravulizumab Alexion Pharma/AstraZeneca mAb i.v. Commercialized, phase III aHUS
Crovalimab Roche mAb s.c. Phases II–III aHUS
C3 Inhibition of the binding of C3 to the C3bBb and thus of the cleavage of C3 Pegcetacoplan Apellis Pharma/SOBI Pegylated peptide s.c. Phase III C3G, IgAN, MN
Factor B Inhibition of the serine protease FB and thus of the cleavage of C3 and C5 Iptacopan Novartis Small molecule Oral Phases II–III aHUS, C3G, MN, IgAN
Factor D Inhibition of the cleavage of FB Danicopan A Alexion Pharma/AstraZeneca Small molecule Oral Phases II–III C3G
MASP2 Inhibition of the serine protease MASP2 Narsoplimab Omeros mAb i.v. Phase II IgAN
C5a receptor Inhibition of the binding of C5a to its receptor Avacopan Chemocentrix Small molecule Oral Phase III ANCA-associated vasculitis aHUS

aHUS, atypical hemolytic uremic syndrome; ANCA, anti-neutrophil cytoplasmic autoantibody; C3G, C3 glomerulopathy; IgAN, IgA nephropathy; mAb, monoclonal antibody; MN, membranous nephropathy; s.c., subcutaneously.