MEDI-507
Drug0.012 mg/kg given intravenously on Study Days 0, 3, 6 and 9
NCT Number: NCT00813618
To assess the safety of escalating dose levels of MEDI-507 in pediatric stem cell and bone marrow allograft recipients who have at least Grade II GvHD.
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Notify Me2 year–17 year
All sexes
Interventional
Phase 1
Children's Hospital, Birmingham, Alabama, United States
This is a Phase I, open-label dose escalation trial of MEDI-507 in pediatric SCT and BMT recipients with at least Grade II acute GvHD. All patients will receive steroid therapy and MEDI-507 for treatment of GvHD
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
0.012 mg/kg given intravenously on Study Days 0, 3, 6 and 9
Time frame: Through Study Day 44
Time frame: Through Study Day 364
MedImmune LLC
Industry
Phase I Study of MEDI 507 in the Treatment of Pediatric Patients With at Least Grade II Acute Graft-Versus-Host Disease (GvHD)
Acronym: Pediatric GvHD
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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