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RecruitingNCT00603330Updated May 9, 2024

Mesenchymal Stem Cell Infusion as Treatment for Steroid-Resistant Acute Graft Versus Host Disease (GVHD) or Poor Graft Function

A Phase 2 interventional study of Mesenchymal stem cells in Graft-versus-host Disease, Poor Graft Function and Low Donor T-cell Chimerism, sponsored by University of Liege. Recruiting at 12 sites in 2 countries. Per ClinicalTrials.gov, last updated 2024-05-09.

Sponsored by University of Liege · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Aug 2024, 2 years 2 months ago, but the record still lists the study as recruiting.
  • Started Jan 2008; still recruiting 18 years 9 months later.
Phase
Phase 2
Study type
Interventional
Enrollment
100
Allocation
Non-randomized
Sex
All
01

Study summary

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.

Read the detailed description

Part 1: complete recruitment Part 2: complete recruitment Part 3: recruiting

02

Conditions studied

  • Graft-versus-host Disease
  • Poor Graft Function
  • Low Donor T-cell Chimerism

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Keywords

  • Mesenchymal stem cells
  • Graft-versus-host disease
  • Poor graft function
  • Chimerism
  • Hematopoietic cell transplantation recipients
  • Low donor T-cell chimerism
03

In context

Graft vs Host Disease

806 studies on the registry are indexed under Graft vs Host Disease; 138 are open to participants now.

This study's planned enrollment of 100 is above the median of 35 across 637 interventional studies indexed under Graft vs Host Disease.

Browse Graft vs Host Disease studies →

Lead sponsor

University of Liege is the lead sponsor of 242 studies on the registry; 46 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

Patient eligibility criteria

  1. Male or female of any age.
  2. Previous allogeneic transplantation (related or unrelated donor, any degree of HLA matching) or autologous transplantation (for part 2 only) of HSC at any time before.
  3. Any source of HSC (marrow, PBSC, cord blood) and any conditioning regimen.
  4. Informed consent given by donor or his/her guardian if of minor age.
  5. Additional criteria for each part of the protocol:

Part 1: MSC for steroid-refractory grade II-IV acute GVHD

  1. Allogeneic transplantation.
  2. Grade II-IV acute GVHD (see appendix A for acute GVHD grading) de novo or following DLI.
  3. Acute GVHD refractory to mPDN 2 mg/kg/day or equivalent, defined as

    • progression of GVHD on day 3 after initiation of steroids
    • no improvement of GVHD on day 7 after initiation of steroids
    • absence of complete resolution of acute GVHD on day 14 after initiation of steroids
    • relapse of acute GVHD during or after steroid taper.
  4. Ongoing therapy with Ciclosporine or Tacrolimus at therapeutic doses.
  5. Patient may have received previously any other form of treatment for acute GVHD, but no new treatment started within 1 month of study entry.

Part 2: MSC for poor graft function (PGF)

  1. Allogeneic or autologous transplantation.
  2. Cytopenia in 2 or 3 lineages:

    • Hb \< 8.0 g/dL and reticulocytes \< 1%, with or without transfusion
    • Plt \< 20,000/µL without transfusion
    • Neutrophils \< 500/µL, without G-CSF administration

    OR severe cytopenia in 1 lineage:

    • RBC transfusion dependent (if autologous transplantation; despite EPO administration if allogeneic transplantation)
    • Plt transfusion dependent
    • Neutrophils \< 500/µL despite G-CSF administration
  3. Cytopenia duration ≥ 2 weeks beyond day 28 after autologous HCT, or day 42 (day 60 for cord blood transplantation) after allogeneic HCT.
  4. Cytopenia is not related to CMV or other infection, myelosuppressive/toxic drugs, renal failure, peripheral cell destruction or other identifiable cause.
  5. In case of HLA-identical related donor and full donor chimerism, patient can only be included if a boost of donor CD34+ cells has been unsuccessful or is not feasible.

Part 3: MSC + DLI for poor donor T-cell chimerism

  1. Nonmyeloablative allogeneic transplantation.
  2. Donor T-cell chimerism \< 50% for at least 2 consecutive weeks beyond day 21 after HCT OR

    • 20% decrease in donor T-cell chimerism with the second value \< 50%.

MSC donor inclusion criteria

  1. Related to the recipient (sibling, parent or child) or unrelated.
  2. Male or female.
  3. Age > 16 yrs (no age limit if same as HSC donor).
  4. No HLA matching required.
  5. Fulfills generally accepted criteria for allogeneic HSC donation.
  6. Informed consent given by donor or his/her guardian if of minor age.

Exclusion criteria

Exclusion Criteria:

Patient exclusion criteria

  1. HIV positive.
  2. Active uncontrolled infection at time of scheduled MSC infusion.
  3. Relapsing or progressing malignancy.

MSC donor exclusion criteria

  1. HIV positive
  2. Known allergy to Lidocaine
  3. If donor other than HSC donor : any risk factor for transmissible infectious diseases.
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    1

    MSC infusion for steroid-refractory grade II-IV acute GVHD. In this arm, 4 x 10E6 MSC/Kg BW of the recipient will be injected during the first hour after thawing.

    Biological: Mesenchymal stem cells

  • Experimental
    2

    MSC infusion for poor graft function. In this arm, 2 x 10E6 MSC/Kg BW of the recipient will be injected during the first hour after thawing.

    Biological: Mesenchymal stem cells

  • Experimental
    3

    MSC + DLI for poor donor T-cell chimerism after allogeneic HCT. In this arm, 2 x 10E6 MSC/Kg BW of the recipient will be injected during the first hour after thawing.

    Biological: Mesenchymal stem cells

Interventions

  • BiologicalMesenchymal stem cells

    Mesenchymal Stem Cell infusion

06

What researchers measure

Primary outcomes

  1. Arm 1. Efficacy of MSC infusion as treatment for steroid-resistant grade II - IV acute GVHD.

    Time frame: 30 days

  2. Arm 2. Efficacy of MSC infusion as treatment for poor graft function

    Time frame: 180 days

  3. 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

Secondary outcomes

  1. Toxicity of MSC infusion

    Time frame: 180 days

07

Study locations

11 of 12 sites recruiting
  • UZA
    Edeghem, Antwerpen 2650, Belgium
    • Zwi Berneman, MD, PhD · Contact · zwi.berneman@uza.be · 32(03)8213250
    • Zwi Berneman, MD, PhD · Principal investigator
    Recruiting
  • Hôpital des enfants Reine Fabiola
    Brussels, Brabant 1020, Belgium
    • Alice Ferster, MD · Contact · alice.ferster@huderf.be · 32(02)4773283
    • Alice Ferster, MD · Principal investigator
    Recruiting
  • AZ VUB Jette
    Brussels, Brabant 1090, Belgium
    • Rik Schots, MD, PhD · Contact · Rik.Schots@uzbrussel.be · 32 (02) 4763105
    • Rick Schots, MD, PhD · Principal investigator
    Recruiting
  • Cliniques universitaires Saint-Luc- Université Catholique de Louvain
    Brussels, Brabant 1200, Belgium
    Recruiting
  • AZ Gasthuisberg Leuven
    Leuven, Flamish Brabant 3000, Belgium
    Recruiting
  • UZ Gent
    Gent, Flanders Ost 9000, Belgium
    • Lucien Noens, MD, PhD · Contact · Lucien.Noens@Ugent.be · 32(09) 332 21 31
    • Lucien Noens, MD, PhD · Principal investigator
    Recruiting
  • Hôpital de Jolimont
    Haine St Paul, Hainaut 7100, Belgium
    Recruiting
  • Cliniques Universitaires Mont-Godinne
    Yvoir, Namur 5530, Belgium
    Recruiting
  • AZ St Jan
    Brugge, West Flanders 8000, Belgium
    Recruiting
  • Hôpital Stuyvenberg
    Antwerpen, 2060, Belgium
    • Pierre Zachée, MD, PhD · Contact · pierre.zachee@zna.be · 32(03)2177111
    • Pierre Zachée, MD, PhD · Principal investigator
    Recruiting
  • CHU Sart Tilman
    Liege, 4000, Belgium
    • Yves Beguin, MD/PhD · Contact · yves.beguin@chu.ulg.ac.be · 32-4-366 72 01
    • Frederic Baron, MD/PhD · Contact · F.Baron@ulg.ac.be · 32-4-366 72 01
    • Yves Beguin, MD, PhD · Principal investigator
    • Frederic Baron, MD, PhD · Principal investigator
    • Chantal Lechanteur, PhD · Principal investigator
    • Etienne Baudoux, MD · Sub investigator
    • Evelyne Willems, MD · Sub investigator
    • Pascale Frère, MD, PhD · Sub investigator
    • Bernard De Prijck, MD · Sub investigator
    Recruiting
  • University Hospital Maastricht
    Maastricht, Limburg 6200, Netherlands
    Not yet recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 9, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00603330
Lead sponsor
University of Liege
Collaborators
KU Leuven, Maastricht University Medical Center, Ziekenhuis Netwerk Antwerpen (ZNA), University Hospital, Antwerp, University Hospital, Ghent, AZ-VUB, AZ Sint-Jan AV, Cliniques universitaires Saint-Luc- Université Catholique de Louvain, University Hospital of Mont-Godinne, Jolimont Hospital Haine Saint Paul, Queen Fabiola Children's University Hospital
Responsible party
Yves Beguin (Prof, University of Liege) — Principal investigator
First posted
Jan 29, 2008
Start date
Jan 2008
Primary completion
Aug 2024 (estimated)
Completion
Aug 2024 (estimated)
Last update
May 9, 2024

Study contacts

Yves Beguin, MD, PhD
Contact
yves.beguin@chu.ulg.ac.be
32-4-366 72 01
Frederic Baron, MD, PhD
Contact
F.Baron@ulg.ac.be
32-4-366 72 01
Yves Beguin, MD, PhD
study chair · CHU-ULg
Frédéric Baron, MD, PhD
study chair · CHU-ULg
Johan Maertens, MD
principal investigator · KU Leuven
Harry Schouten, MD
principal investigator · Maastricht University Medical Center
Pierre Zachée, MD
principal investigator · Stuyvenberg Hospital Antwerpen
Zwi Berneman, MD
principal investigator · UZA Antwerpen
Lucien Noens, MD, PhD
principal investigator · UZ-Gent
Rick Schots, MD, PhD
principal investigator · AZ VUB Jette
Dominik Selleslag, MD
principal investigator · AZ St. Jan Bugge
Augustin Ferrant, MD, PhD
principal investigator · UCL St. Luc Brussels
Chantal Doyen, MD
principal investigator · Cliniques Universitaires Mont-Godinne at Yvoir
Nicole Straetmans, MD
principal investigator · Hôpital de Jolimont at Haine-St-Paul
Nicole Ferster, MD
principal investigator · Hôpital des enfants Reine Fabiola at Brussels

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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