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Clinical trialNCT01045382TerminatedPhase 2Interventional

MSC and HSC Coinfusion in Mismatched Minitransplants

SponsorUniversity of LiegeEnrollment39Hodgkin's DiseaseLeukemia, Lymphoblastic, AcuteLeukemia, Lymphocytic, ChronicLeukemia, Myelocytic, ChronicLeukemia, Myeloid, AcuteLymphoma, Non-Hodgkin+3 more conditions
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The present project aims at evaluating the capacity of MSC to improve one-year overall survival of patients transplanted with HLA-mismatched PBSC from related or unrelated donors after non-myeloablative conditioning. Co-infusion of MSC has been shown to facilitate engraftment of hematopoietic stem cell (HSC) in an immunodeficient mouse model. In addition, it has been shown that infusion of third party MSC in HSC transplantation could be successfully used as treatment for grade II-IV steroid-refractory acute graft versus host disease. One hundred and twenty patients with HLA-mismatched donors will be included over 6 years at multiple centers across Belgium through the transplant committee of the Belgian Hematological Society. The conditioning regimen will consist of fludarabine and 2 Gy TBI, followed by the infusion of donor HSC. Patients will be randomized 1/1 in double-blind fashion to receive or not MSC (1.5-.3.0 x106/kg) from third-party (either haploidentical family members or unrelated volunteer) donors on day 0. Postgrafting immunosuppression will combine tacrolimus and MMF. Except for the collection, expansion and infusion of MSC, the clinical management of the patient will not differ from that of routine NM-HCT.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

10 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Belgium
  • Uza

    Edegem, Antwerpen, Belgium

  • St-Luc Ucl

    Brussels, Brabant, Belgium

  • Az Gasthuisberg Leuven

    Leuven, Flamish Brabant, Belgium

  • Uz Gent

    Ghent, Flanders Ost, Belgium

  • Az St-Jan

    Bruges, Flanders West, Belgium

  • Cliniques Universitaires Mont-Godinne

    Yvoir, Namur, Belgium

  • Hôpital Stuyvenberg

    Antwerp, Belgium

  • Bordet Institute

    Brussels, Belgium

  • Vrije Universiteit Brussel

    Brussels, Belgium

  • Chu-Ulg

    Liège, Belgium

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Mesenchymal stem cells
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Jul 2010
Primary completion
31 Aug 2021
Completion
31 Aug 2021
Last update posted
8 Sept 2021
Registered enrollment
39
Registry id
NCT01045382

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.