Clinical Trials Logo

Clinical Trial Summary

Ongoing safety assessment follow-up to Protocol MSB-GVHD001 (NCT02336230) of remestemcel-L treatment in pediatric participants with acute graft versus host disease (aGVHD), following allogeneic hematopoietic stem cell transplant (HSCT), that have failed to respond to treatment with systemic corticosteroid therapy.


Clinical Trial Description

This is a safety follow-up study through 180 days of remestemcel-L treatment in participants who took part in MSB-GVHD001. This study will also explore duration of response over time. Participants who took part in in MSB-GVHD001 and received at least one dose of remestemcel-L as outlined in that protocol will be evaluated at baseline (Day 100) and at Days 120, 140, 160 and 180 for safety endpoints. Participants who took part in Protocol MSB-GVHD001 and received the first 8 doses of remestemcel-L as outlined in that protocol will be evaluated at baseline (Day 100) and at Days 120, 140, 160 and 180 after initial remestemcel-L infusion for evidence of duration of response over time. ;


Study Design


Related Conditions & MeSH terms

  • Grade B Acute Graft Versus Host Disease
  • Grade C Acute Graft Versus Host Disease
  • Grade D Acute Graft Versus Host Disease
  • Graft vs Host Disease

NCT number NCT02652130
Study type Interventional
Source Mesoblast, Ltd.
Contact
Status Completed
Phase Phase 3
Start date October 28, 2015
Completion date June 15, 2018