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J Comp Eff Res ; 11(13): 969-985, 2022 09.
Artigo em Inglês | MEDLINE | ID: mdl-35796199

RESUMO

Aim: Paroxysmal nocturnal hemoglobinuria (PNH) is a rare blood disorder characterized by hemolytic anemia, bone marrow failure and thrombosis. We evaluated, the cost-effectiveness of pegcetacoplan, a novel proximal C3 inhibitor, versus ravulizumab in patients with PNH and hemoglobin levels <10.5 g/dl despite eculizumab treatment in the UK healthcare and social services setting. Materials & methods: A Markov cohort framework model, based on the data from the pivotal trial of pegcetacoplan (PEGASUS/NCT03500549), evaluated lifetime costs and outcomes. Patients transitioned through 3 PNH hemoglobin level/red blood cell transfusion health states. Results: Pegcetacoplan provides lower lifetime costs/greater quality-adjusted life years (£6,409,166/14.694QALYs, respectively) versus ravulizumab (£6,660,676/12.942QALYs). Conclusion: Pegcetacoplan is associated with enhanced anemia control, greater QALYs and reduced healthcare costs versus ravulizumab in the UK healthcare and social services setting.


Assuntos
Hemoglobinúria Paroxística , Anticorpos Monoclonais Humanizados , Ensaios Clínicos como Assunto , Análise Custo-Benefício , Hemoglobinas , Hemoglobinúria Paroxística/tratamento farmacológico , Humanos , Peptídeos Cíclicos , Reino Unido
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