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ATYPICAL HAEMOLYTIC URAEMIC SYNDROME

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Oct 15 / Roche and Genentech
Real-World Treatment Patterns Among Patients With Paroxysmal Nocturnal Hemoglobinuria Initiating Eculizumab and Ravulizumab: A US Claims Analysis
C5 inhibitors are standard of care for PNH treatment in the US, with intravenous eculizumab and ravulizumab having transformed clinical outcomes. To ensure optimal care for patients given the recent FDA approvals of newer complement inhibitors, this poster reports results from a US claims analysis on real-world treatment patterns in patients with PNH who initiated eculizumab or ravulizumab.

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May 23 / Roche and Genentech
Crovalimab▼: Patient preferences and ongoing Phase III COMMUTE trials in acute haemolytic uraemic syndrome (aHUS)
Crovalimab▼ was shown to be well tolerated and efficacious in patients with PNH in the global, randomized Phase III COMMODORE 1 and 2 studies, and is currently being evaluated in the ongoing global, Phase III, single-arm COMMUTE-a and COMMUTE-p trials in aHUS. This poster reports results patient preference data from COMMODORE 1 and 2 patients who were treated with crovalimab▼ and eculizumab, as well as the study designs of COMMUTE-a and COMMUTE-p.

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Nov 4 / Roche and Genentech
Phase III COMMODORE trials of crovalimab▼ in paroxysmal nocturnal hemoglobinuria (PNH): impact on kidney function
Crovalimab▼ was evaluated as a treatment for patients with paroxysmal nocturnal hemoglobinuria in the Phase III COMMODORE 1, 2, and 3 studies. Crovalimab▼ is also being evaluated for atypical hemolytic uremic syndrome (aHUS), a complement-mediated disorder that directly affects the kidneys, in the COMMUTE-a and COMMUTE-p studies. This poster describes an analysis of kidney function in patients from the COMMODORE studies to further assess the feasibility of using crovalimab▼ to treat patients with aHUS.

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Jun 16 / Roche and Genentech
Rapid complement inhibition with the C5 inhibitor crovalimab▼: timing analysis using animal model and COMPOSER trial data
Both atypical hemolytic uremic syndrome (aHUS) and paroxysmal nocturnal hemoglobinuria (PNH) are disorders characterized by dysregulated complement activation. In this analysis, time to complete complement inhibition after the first crovalimab▼ intravenous dose was evaluated using results from in vivo models of cynomolgus monkeys and from patients with paroxysmal nocturnal hemoglobinuria in the Phase I/II COMPOSER trial. The ongoing Phase III COMMUTE-a and COMMUTE-p trials evaluating crovalimab▼ in adult and pediatric patients with aHUS are also described.

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Nov 3 / Roche and Genentech
Two Phase III trials evaluating crovalimab in patients with atypical hemolytic uremic syndrome (aHUS): COMMUTE-a and COMMUTE-p
Atypical hemolytic uremic syndrome (aHUS) is a life-threatening complement-mediated disorder. Currently approved treatments include C5 inhibitors, which although effective, impose a significant treatment burden on patients, about 50% of whom are < 18 years old. Two Phase III studies, COMMUTE-a and COMMUTE-p will evaluate the efficacy and safety of crovalimab (anti-C5) in adult/adolescent and pediatric patients with aHUS, respectively.

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Jun 24 / Roche and Genentech
Two Phase III trials evaluating crovalimab in patients with atypical hemolytic uremic syndrome (aHUS): COMMUTE-a and COMMUTE-p
Atypical hemolytic uremic syndrome (aHUS) is a life-threatening complement-mediated disorder. Currently approved treatments include C5 inhibitors, which although effective, impose a significant treatment burden on patients, about 50% of whom are < 18 years old. Two Phase III studies, COMMUTE-a and COMMUTE-p will evaluate the efficacy and safety of crovalimab (anti-C5) in adult/adolescent and pediatric patients with aHUS, respectively.

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