A Pilot Study of Efgartigimod for Immune-mediated Thrombotic Thrombocytopenic Purpura (iTTP)

Обзор

Immune-mediated Thrombotic thrombocytopenic purpura (iTTP) is a rare, autoimmune disorder characterized by life-threatening episodes of thrombocytopenia, microangiopathic hemolytic anemia and organ damage. Patients have an unpredictable course punctuated by relapses associated with autoantibody-mediated (primarily IgG) depletion of ADAMTS13, a key regulator of coagulation. ADAMTS13 deficiency during remission has been associated with increased risk of relapse, but also, and potentially more devastating, ischemic stroke. Until recently, it was presumed that rituximab (a monoclonal antibody targeting B cells) improved relapse-free survival in most patients, but this was based on findings from very small studies. Given concern about stroke and relapse risk, preventive immunosuppression with rituximab has also recently come into practice for patients with falling ADAMTS13 activity (ADAMTS13-relapse). It is expected that following efgartigimod therapy, there will be a rise in ADAMTS13 activity to the normal range that will be sustained during the treatment period. Following withdrawal of therapy, it is expected that most participants will experience a fall in ADAMTS13 activity, demonstrating the safety and efficacy in efgartigimod to reliably but temporarily reduce pathogenic antibodies. This would demonstrate the potential efficacy for efgartigimod as a maintenance therapy to safely prevent relapse of iTTP to be further explored in a larger efficacy study.

Вмешательства

• Препарат efgartigimod
  intravenous efgartigimod weekly with monitoring of ADAMTS13 activity for 8 weeks, followed by an observational period of 8 weeks or until treatment failure.

Первичные конечные точки

• safety of efgartigimod by the incidence of relapse [Срок оценки: 8 weeks post-intervention]
• safety and tolerability of efgartigimodhistorical rituximab arm [Срок оценки: 8 weeks post-intervention]
• efficacy of efgartigimod to achieve a normal ADAMTS13 activity by Day 60 of the study [Срок оценки: 60 days]
• efficacy of efgartigimod to prevent the need for other preemptive therapy to rescue severe ADAMTS13 deficiency [Срок оценки: 8 weeks post-intervention]

Вторичные конечные точки (2)

• the efficacy of efgartigimod to raise ADAMTS13 activity more rapidly than historically treated patients with rituximab [Срок оценки: Day 60 and day 90]
• the efficacy of efgartigimod to deplete pathogenic ADAMTS13 antibodies [Срок оценки: 8 weeks post-intervention]

Критерии участия

Критерии включения

• Subject must provide a signed informed consent form
• Subject is 18 years or older at the time of screening
• Subject has a prior history of iTTP as defined by the presence of ADAMTS13 activity < 10% with ADAMTS13 antibodies or inhibitor, thrombocytopenia (platelet count < 100) and microangiopathic hemolytic anemia (defined by the presence of schistocytes on blood smear)
• Subject is in clinical remission from iTTP (normal platelet count) for at least 90 days
• Subject has ADAMTS13 activity < 70% and > 30% on 2 separate occasions separate by at least 7 days
• Subject is at least 6 months from last dose of rituximab or other intravenous immunosuppression
• If taking other oral immunosuppressants, no change in dose for at least 60 days
• Female subjects of childbearing potential must present with a negative pregnancy test and agree to employ highly effective birth control measures for duration of study.

Sexually active male subjects must agree to use an effective method of contraception for the duration of the study

Критерии исключения

• Subject has been diagnosed with cTTP
• Subject has been exposed to another investigational product within 30 days prior to enrollment or is scheduled to participate in another clinical study involving investigational product or investigational device during the course of the study
• Subject is unable to understand the nature, scope, and possible consequences of the study.
• Subject is pregnant or lactating
• Subject has a known life-threatening hypersensitivity reaction to efgartigimod

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Не применимо

Модель

Одна группа

Маскирование

Открытое

Основная цель

Лечение

Центры проведения

США · 1 центр

• University of Minnesota — Minneapolis

Идентификаторы

NCT: NCT06831058 · HOT-2024-32825

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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