Actively Recruiting

Phase 2
Age: 16Years - 70Years
All Genders
NCT04888741

Methods of T Cell Depletion Trial (MoTD)

Led by University of Birmingham · Updated on 2026-05-05

400

Participants Needed

17

Research Sites

339 weeks

Total Duration

On this page

Sponsors

U

University of Birmingham

Lead Sponsor

T

The Jon Moulton Charity Trust

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Methods of T Cell Depletion Trial (MoTD)

Who Can Participate

Age: 16Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Availability of a suitably matched unrelated donor (9/10 or 10/10)
  • Planned to receive one of the following reduced intensity conditioning protocols: Fludarabine-Melphalan, BEAM or LEAM, Fludarabine-Busulphan, or Fludarabine-Treosulfan
  • Planned use of peripheral blood stem cells for transplantation
  • Planned allogeneic stem cell transplant for specified haematological malignancies including AML, ALL, CMML (<10% blasts), MDS (<10% blasts), NHL, HL, MM, CLL, CML in 1st or 2nd chronic phase, or Myelofibrosis
  • Age between 16 and 70 years
  • Females and males of reproductive potential must agree to use appropriate, highly effective contraception from starting therapy until 12 months after transplant
Not Eligible

You will not qualify if you...

  • Use of any graft manipulation method not defined by the protocol (except storage of future donor lymphocyte infusion)
  • Use of alemtuzumab or any T-cell depletion method outside the study protocol
  • Known allergy to study drugs or history of rabbit hypersensitivity
  • Pregnant or lactating women
  • Adults of reproductive potential unwilling to use effective contraception during the study period
  • Life expectancy less than 8 weeks
  • Active hepatitis B or C infection
  • Organ dysfunction including left ventricular ejection fraction below 45%, glomerular filtration rate below 50ml/min, bilirubin over 50 µmol/l, or liver enzymes (AST/ALT) more than 3 times the upper limit of normal
  • Participation in COSI or ALL-RIC trials
  • Contraindications to study drugs as per their safety information
  • Other significant systemic dysfunction or disorders that could jeopardise patient safety during the trial

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 17 locations

1

University Hospital of Wales

Cardiff, Wales, United Kingdom, CF14 4XW

Actively Recruiting

2

Queen Elizabeth Hospital

Birmingham, United Kingdom, B15 2GW

Actively Recruiting

3

Bristol Haematology and Oncology Centre

Bristol, United Kingdom, BS2 8ED

Actively Recruiting

4

Addenbrookes Hospital

Cambridge, United Kingdom, CB2 0QQ

Actively Recruiting

5

Queen Elizabeth Hospital Glasgow

Glasgow, United Kingdom, G51 4TF

Actively Recruiting

6

St Jame's University Hospital

Leeds, United Kingdom, LS9 7TF

Actively Recruiting

7

University College London Hospital

London, United Kingdom, NW1 2BU

Actively Recruiting

8

King's College Hospital

London, United Kingdom, SE5 9RS

Actively Recruiting

9

Hammersmith Hospital

London, United Kingdom, W12 0HS

Actively Recruiting

10

Manchester Royal Infirmary

Manchester, United Kingdom, M13 9WL

Actively Recruiting

11

The Christie

Manchester, United Kingdom, M20 3QH

Actively Recruiting

12

Freeman Hospital

Newcastle upon Tyne, United Kingdom, NE7 7DN

Actively Recruiting

13

Nottingham City Hospital

Nottingham, United Kingdom, NG5 1PB

Actively Recruiting

14

Churchill Hospital

Oxford, United Kingdom, OX3 7LE

Actively Recruiting

15

Derriford Hospital

Plymouth, United Kingdom, PL6 8DH

Actively Recruiting

16

Royal Hallamshire Hospital

Sheffield, United Kingdom, S102JF

Actively Recruiting

17

The Royal Marsden Hospital

Sutton, United Kingdom, SM2 5PT

Actively Recruiting

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Research Team

M

MoTD Trial

CONTACT

A

Andrea Dr Hodgkinson

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

3

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