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Precision Medicine for Stem Cell Transplantation

Sponsor: University of Manchester

NCT ID: NCT05567289

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Blood sample collection (procedure), Bone marrow aspirate (procedure)
How long the study runs
Study runs about 62 months (dates as stated)
About the drug or intervention
Blood sample collection — procedure: Enrolled patients will undergo sequential blood collection beginning prior to conditioning, then on the day of transplant (day 0), followed by days 7, 14, 21, 28, 56 (2 months) and 90 (3 months) post-transplant. · Bone marrow aspirate — procedure: Bone marrow aspirates taken within this period as part of routine care will also be collected, these are typically performed around day 100 and whenever there is suspicion of disease recurrence.
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
Not specified
Who
All
Number of participants
300
Started
2023-06-06
Last checked
2025-01

Plain English Summary

What is this study?

  • • Testing a new treatment for haematopoietic stem cell transplantation
  • • Clinical study - 300 participants
  • • A study of patients undergoing haematopoietic stem cell transplantation, a procedure in which patients are infused with stem cells from a donor, resulting in a new immune system that eliminates cancer or replaces diseased bone marrow

Who can take part?

  • • Adults
  • • Diagnosed with haematopoietic stem cell transplantation

Where?

  • • Manchester - Manchester Royal Infirmary
  • • Manchester - Royal Manchester Children's Hospital
  • • Manchester - The Christie NHS Foundation Trust

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

A study of patients undergoing haematopoietic stem cell transplantation, a procedure in which patients are infused with stem cells from a donor, resulting in a new immune system that eliminates cancer or replaces diseased bone marrow. This study aims to develop new blood tests that predict the onset of acute graft-versus-host disease (aGvHD) and leukaemia relapse, two life-threatening complications that frequently limit the success of treatment. Predictive tests would allow doctors to individualise prophylaxis and intervene early to abort complications before they develop. The study will also create a large collection of clinically annotated blood samples from 300 transplant recipients to support future research and provide a resource to the transplant research community.

More detail

Precision Medicine for Stem Cell Transplantation (PM-SCT) is a prospective cohort study of patients undergoing allogeneic haematopoietic stem cell transplantation (HSCT). The study aims to develop novel biomarkers that predict the onset of acute graft-versus-host disease (aGvHD) and post-transplant relapse of acute myeloid leukaemia (AML). The study will also build a collection of clinically annotated longitudinal blood samples from 300 HSCT recipients to support additional mechanistic research and provide a resource to the transplant research community. Patients will be recruited and consented prior to admission for HSCT. Enrolled patients will undergo sequential blood collection beginning prior to conditioning, then on the day of transplant (day 0), followed by days 7, 14, 21, 28, 56 (2 months) and 90 (3 months) post-transplant. Samples will be collected, processed, and stored by the MCRC Biobank. The period of observation for each patient is 6-months. Clinical data will be collected prospectively: on admission, with each blood sample, and at 6-months post-transplant. Bone marrow aspirates taken within this period as part of routine care will also be collected, these are typically performed around day 100 and whenever there is suspicion of disease recurrence. The study aims to identify all patients who develop aGvHD, collecting an additional blood sample at the onset of treatment for those who receive systemic corticosteroids (PO or IV steroid equivalent to ≥0.5mg/kg prednisolone). Additional clinical data will be collected at treatment onset and 7, 14, 21 and 28 days after starting systemic corticosteroids. These assessments will provide the clinical data necessary to establish diagnostic confidence, severity at onset/peak, response to treatment and outcome.

Haematopoietic Stem Cell Transplantation

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What we know so far

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Still need:

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: Not specified
  • Who can join: All genders

What the study is looking for

  • ✓Any recipient of allogeneic haematopoietic stem cell transplantation (HSCT)
  • ✓Children/infants may participate, there is no age restriction
  • ✓Patients participating in other clinical trials remain eligible

Who cannot take part

  • ✗Weight \<5kg
  • ✗Recipients of autologous stem cell transplants
See the full criteria
Inclusion Criteria: * Any recipient of allogeneic haematopoietic stem cell transplantation (HSCT) * Children/infants may participate, there is no age restriction * Patients participating in other clinical trials remain eligible Exclusion Criteria: * Weight \<5kg * Recipients of autologous stem cell transplants

Where Is This Study? (3 UK sites)

Manchester Royal Infirmary

Manchester m13 9wl, United Kingdom

Recruiting
Site contact (verified)
Fiona DignanPrincipal Investigator

Royal Manchester Children's Hospital

Manchester m139wl, United Kingdom

Recruiting
Site contact (verified)
Robert WynnPrincipal Investigator

The Christie NHS Foundation Trust

Manchester M20 4BX, United Kingdom

Recruiting
Site contact (verified)
Adrian BlloorPrincipal Investigator

How to Get in Touch

Mark Williams

Sponsor contact

CONTACT

+441613063240 mark.williams-4@cruk.manchester.ac.uk

Abbey Walker

Sponsor contact

CONTACT

0161 446 8201 abbey.walker@manchester.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2025-01