Clinical Trial Matcher

NCT04888741

Methods of T Cell Depletion Trial (MoTD)

Recruiting · Phase 2 · University of Birmingham · registry updated 2026-05-05

Inclusion and exclusion lines below are quoted from ClinicalTrials.gov. No match score is shown, because a score needs a person's age, biomarkers, and treatment dates. Confirm the record with the study team.

A multi-centre phase II trial of GvHD prophylaxis following unrelated donor stem cell transplantation comparing Thymoglobulin vs. Calcineurin inhibitor or Sirolimus-based post-transplant cyclophosphamide.

Inclusion

  • Availability of suitably matched unrelated donor (9/10 or 10/10)
  • Planned to receive one of the following RIC protocols:
  • Fludarabine-Melphalan (Fludarabine 120-180mg/m2 IV; melphalan ≤ 150mg/m2 IV)
  • BEAM or LEAM (carmustine 300mg/m2 IV or lomustine 200mg/m2 IV with: etoposide 800 mg/m2 IV; cytarabine 1600mg/m2 IV; melphalan 140mg/m2 IV)
  • Fludarabine-Busulphan (Fludarabine 120-180mg/m2 IV; Busulphan ≤ 8mg/kg PO or 6.4mg/kg IV)
  • Fludarabine- Treosulfan (Fludarabine 150mg/m2 IV; Treosulfan 30g/m2 IV)

Exclusion

  • Use of any method of graft manipulation (excluding storage of future DLI)
  • Use of alemtuzumab or any method of T cell depletion except those that are protocol-defined
  • Known hypersensitivity to study drugs or history of hypersensitivity to rabbits
  • Pregnant or lactating women
  • Adults of reproductive potential not willing to use appropriate, highly effective, contraception during the specified period
  • Life expectancy \<8 weeks

Open NCT04888741 on ClinicalTrials.govAll conditions