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:
- 1 month 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 despite initial management of any triggering condition.
- Body weight ≥ 5 kilograms.
- Female participants of childbearing potential and male participants with female partners of childbearing potential must use highly effective contraception starting at Screening and continuing until at least 8 months after the last dose of ravulizumab.
- Participants must be vaccinated against meningococcal infections if clinically feasible, according to institutional guidelines for immune reconstitution after HSCT. Participants must be re-vaccinated against Haemophilus influenzae type b and Streptococcus pneumoniae if clinically feasible, according to the institutional guidelines for immune reconstitution after HSCT. All participants should be administered coverage with prophylactic antibiotics according to institutional post-transplant infection prophylaxis guidances, including coverage against Neisseria meningitidis for at least 2 weeks after meningococcal vaccination. Participants who cannot receive meningococcal vaccine should receive antibiotic prophylaxis coverage against Neisseria meningitidis the entire Treatment Period and for 8 months following the final dose of ravulizumab.
EXCLUSION CRITERIA
Exclusion Criteria:
- Known familial or acquired 'a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13' deficiency (activity < 5%).
- Known Shiga toxin-related hemolytic uremic syndrome.
- Positive direct Coombs test.
- Diagnosis or suspicion of disseminated intravascular coagulation.
- Known bone marrow/graft failure.
- Diagnosis of veno-occlusive disease (VOD).
- Human immunodeficiency virus (HIV) infection (evidenced by HIV-1 or HIV-2 antibody titer).
- Unresolved meningococcal disease.
- Presence of sepsis requiring vasopressor support.
- Pregnancy or breastfeeding.
- Hypersensitivity to murine proteins or to 1 of the excipients of Ravulizumab.
- Previously or currently treated with a complement inhibitor.
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 Details
Contition
Thrombotic Microangiopathy
Age
< 17
Phase
PHASE3
Participants Needed
40
Est. Completion Date
May 30, 2025
Treatment Type
INTERVENTIONAL
Sponsor
Alexion Pharmaceuticals, Inc.
ClinicalTrials.gov NCT Identifier
NCT04557735
Study Number
ALXN1210-TMA-314
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