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NOT YET RECRUITING
NCT07826676
PHASE1

Use of Bone Marrow Stem Cells (MesenCell) for the Treatment of Patients With Chronic Graft-versus-host Disease

Sponsor: Pontifícia Universidade Católica do Paraná

View on ClinicalTrials.gov

Summary

The purpose of this Phase I clinical trial is to evaluate the safety and potential treatment response of bone marrow-derived mesenchymal stem cells (MesenCell) in adult patients with moderate or severe chronic graft-versus-host disease (cGVHD) that is refractory to corticosteroid treatment. The main questions it seeks to answer are: * Is MesenCell infusion safe in patients with corticosteroid-refractory chronic graft-versus-host disease? * Can MesenCell treatment improve the clinical response and disease control in these patients? Participants will receive one to three intravenous infusions of MesenCell, according to the study protocol and be followed for 12 months after the last MesenCell infusion.

Official title: Use of Bone Marrow-Derived Mesenchymal Stem Cells (Mesencell) for the Treatment of Patients Undergoing Hematopoietic Progenitor Cell Transplantation Who Developed Refractory Moderate or Severe Chronic Graft-versus-Host Disease: A Phase I Clinical Trial

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2026-10

Completion Date

2028-10

Last Updated

2026-09-17

Healthy Volunteers

No

Interventions

BIOLOGICAL

Mesenchymal Stem Cell Infusion

Administration of Advanced Therapy Medicinal Product in patients with chronic GVHD

Locations (4)

Hospital de Clínicas da Universidade Federal do Paraná

Curitiba, Paraná, Brazil

Pontifícia Universidade Católica do Paraná

Curitiba, Paraná, Brazil

Hospital Nossa Senhora das Graças

Curitiba, Paraná, Brazil

Hospital Erasto Gaertner

Curitiba, Paraná, Brazil