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ABSTRACT: Background
Eculizumab has been approved for atypical haemolytic-uraemic syndrome (aHUS) in Japan since 2013. Post-marketing surveillance enrolled patients with aHUS who received ≥ 1 dose of eculizumab to assess eculizumab safety and effectiveness.Methods
We evaluated serious adverse events and effectiveness endpoints, i.e., haematologic normalization, a decrease of ≥ 25% in serum creatinine (sCr) levels, and complete thrombotic microangiopathy (TMA) response in adult patients with aHUS without other underlying diseases. In addition, the difference of baseline characteristics between patients who did and did not meet effectiveness endpoints was examined.Results
In this safety and effectiveness analysis, 79 adult patients were included; median age was 54.0 years, medi
SUBMITTER: Maruyama S
PROVIDER: S-EPMC11649742 | biostudies-literature | 2024 Nov
REPOSITORIES: biostudies-literature