Study of Ravulizumab in Pediatric Participants With HSCT-TMA
About the study
This study will evaluate the safety, efficacy, pharmacokinetics, and pharmacodynamics of ravulizumab administered by intravenous infusion to pediatric participants, from 1 month to < 18 years of age, with HSCT-TMA. The treatment period is 26 weeks, followed by a 26-week off-treatment follow-up period.
Who can take part
You may be eligible to participate in the study if you meet the following criteria:
INCLUSION CRITERIA
Inclusion Criteria:
- ≥ 28 days of age up to < 18 years of age at the time of signing the informed consent.
- Received HSCT within the past 12 months.
- Diagnosis of TMA that persists for at least 72 hours despite initial management.
- A TMA diagnosis based on meeting the select criteria during the Screening Period and/or <=14 days prior to the Screening Period.
- Body weight ≥ 5 kilograms at Screening or ≤7 days prior to the start of the Screening Period (date of consent).
- Female participants of childbearing potential and male participants with female partners of childbearing potential must use highly effective contraception.
- Participants must be vaccinated against meningococcal infections if clinically feasible. Participants who cannot receive meningococcal vaccine should receive antibiotic prophylaxis.
- Participants or their legally authorized representative must be capable of giving signed informed consent or assent
EXCLUSION CRITERIA
Exclusion Criteria:
- Thrombotic thrombocytopenic purpura (TTP) evidenced by ADAMTS13 deficiency.
- Shiga toxin producing Escherichia coli infection.
- Positive direct Coombs test
- Clinical diagnosis of disseminated intravascular coagulation (DIC)
- Known bone marrow/graft failure.
- Diagnosis of veno-occlusive disease (VOD), regardless of severity.
- Human immunodeficiency virus (HIV) infection
- Unresolved meningococcal disease.
- Presence or suspicion of sepsis (treated or untreated).
- Pregnancy or breastfeeding.
- Respiratory failure requiring mechanical ventilation
- Previously or currently treated with a complement inhibitor
- Participation in an interventional treatment study of any therapy for TMA
Study Locations
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How to Apply
Contact the study center to learn if this study is a good match for you.
Study’s details
Contition
Thrombotic Microangiopathy
Age (in years)
28 - 17
Phase
Phase 3
Participants needed
40
Est. Completion Date
Aug 11, 2025
Treatment type
Interventional
Sponsor
Alexion Pharmaceuticals, Inc.
ClinicalTrials.gov identifier
NCT04557735
Study number
ALXN1210-TMA-314
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