This study will investigate the efficacy and safety of ravulizumab compared to placebo in adult participants with thrombotic microangiopathy (TMA) associated with a trigger. Participants will be randomized to receive either ravulizumab plus best supportive care or placebo plus best supportive care. The treatment period is 26 weeks followed by a 26-week off-treatment follow-up period.
Condition | Thrombotic Microangiopathy |
---|---|
Treatment | Placebo, Best supportive care, Ravulizumab |
Clinical Study Identifier | NCT04743804 |
Sponsor | Alexion Pharmaceuticals |
Last Modified on | 20 October 2022 |
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