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Clinical Trial Summary

Acute GVHD following allogeneic HCT is an immune-triggered process, leading to profound immune dysregulation and organ dysfunction. Despite pivotal advances, aGVHD is one of the leading causes of non-relapse mortality in patients undergoing HCT. Placenta-derived DSCs, isolated from the fetal membrane of maternal origin, are a type of stromal cells with well-characterized immunosuppressive properties. The current study is designed to assess the safety and efficacy of 4 intravenous (IV) doses of ASC930 DSC cells in aGVHD patients.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04883918
Study type Interventional
Source ASC Therapeutics
Contact Clinical Trial Manager, PhD
Phone (408) 495-3891
Email gil.gonen@asctherapeutics.com
Status Not yet recruiting
Phase Phase 2
Start date December 2023
Completion date April 2026

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