The present project aims at investigating the role of MSC for the treatment of patients with Part 1: Steroid-refractory grade II-IV acute GVHD. Part 2: Poor graft function (PGF) Part 3: Low or falling donor T-cell chimerism after allogeneic HCT. This is a multicenter phase II study examining the feasibility and efficacy of this approach.
Part 1: complete recruitment Part 2: complete recruitment Part 3: recruiting
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
100
Mesenchymal Stem Cell infusion
UZA
Edegem, Antwerpen, Belgium
RECRUITINGHôpital des enfants Reine Fabiola
Brussels, Brabant, Belgium
RECRUITINGAZ VUB Jette
Brussels, Brabant, Belgium
RECRUITINGCliniques universitaires Saint-Luc- Université Catholique de Louvain
Brussels, Brabant, Belgium
RECRUITINGAZ Gasthuisberg Leuven
Leuven, Flamish Brabant, Belgium
RECRUITINGUZ Gent
Ghent, Flanders Ost, Belgium
RECRUITINGHôpital de Jolimont
Haine-Saint-Paul, Hainaut, Belgium
RECRUITINGCliniques Universitaires Mont-Godinne
Yvoir, Namur, Belgium
RECRUITINGAZ St Jan
Bruges, West Flanders, Belgium
RECRUITINGHôpital Stuyvenberg
Antwerp, Belgium
RECRUITING...and 2 more locations
Arm 1. Efficacy of MSC infusion as treatment for steroid-resistant grade II - IV acute GVHD.
Time frame: 30 days
Arm 2. Efficacy of MSC infusion as treatment for poor graft function
Time frame: 180 days
Arm 3. Efficacy of MSC infusion followed by donor lymphocyte infusion for preventing graft rejection in patients with low or failing donor T-cell chimerism after allogeneic HCT
Time frame: 180 days
Toxicity of MSC infusion
Time frame: 180 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.