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Tessa Jowell BRAIN MATRIX - Platform Study

Sponsor: University of Birmingham

NCT ID: NCT04274283

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
Matched Tumour and Blood Sample - Research Pathway (other), Matched Tumour and Blood Sample - NHS GMS pathway (other)
How long the study runs
Study runs about 87 months (dates as stated)
About the drug or intervention
Matched Tumour and Blood Sample - Research Pathway — other: For patient's undergoing surgery fresh tissue will be collected from the initial surgery and frozen until shipment to the Oxford BRAIN MATRIX Lab. · Matched Tumour and Blood Sample - NHS GMS pathway — other: Tessa Jowell BRAIN MATRIX centres in England can submit matched tissue and blood samples for Whole Genome Sequencing through the standard of care NHS Genomic Medicine Service pathway via their Genomic Laboratory Hub.
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
16 Years and over
Who
All
Number of participants
1,000
Started
2020-11-24
Last checked
2026-04

Plain English Summary

What is this study?

  • • Testing a new treatment for glioma
  • • Clinical study - 1,000 participants
  • • The main aim of the Tessa Jowell BRAIN MATRIX - Platform Study is to more precisely determine the exact type of tumour patients have by developing the essential infrastructure to provide rapid and accurate molecular diagnosis

Who can take part?

  • • Ages 16 Years and over
  • • Diagnosed with glioma

Where?

  • • Birmingham - Queen Elizabeth Hospital Birmingham, University Hospitals Birmingham NHS Foundation Trust
  • • Cambridge - Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust
  • • Cardiff - Velindre Cancer Centre, Velindre University NHS Trust
  • • Edinburgh - NHS Lothian
  • • +10 more UK sites

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

About This Trial

The main aim of the Tessa Jowell BRAIN MATRIX - Platform Study is to more precisely determine the exact type of tumour patients have by developing the essential infrastructure to provide rapid and accurate molecular diagnosis. A large network of clinical hubs across the United Kingdom, with expertise in managing patients with brain tumours, will be developed. Once established this infrastructure will facilitate the rapid introduction of clinical trials testing targeted therapies tailored to the genetic changes of an individual's tumour.

More detail

Gliomas, a type of brain tumour, are the most common primary tumour of the central nervous system (CNS) and in 2016 there were 5250 deaths from brain tumours in the UK. However, brain tumours are a challenging disease to treat. The tumour's location within the brain and its tendency to grow into nearby brain tissue often make it very difficult to remove the tumour completely with surgery. There is also difficulty in delivering drugs in adequate amounts to the tumour due to the natural defences of the brain. Brain tumours arise due to changes in the DNA and other molecules in cells of the brain. Different types of gliomas can have different changes and these can be used to determine a precise 'molecular diagnosis'. The ultimate goal for the Tessa Jowell BRAIN MATRIX is to learn how to use these molecular changes to more precisely determine what exact type of tumour patients have, and to identify, decide and test whether specific 'targeted' treatments could improve the survival and/or quality of life of patients with brain tumours. Tessa Jowell BRAIN MATRIX is a programme of work, the principal purpose of which is to improve the knowledge of, and treatment for, glioma. The programme will include a Platform Study and subsequent interventional clinical trials. The Tessa Jowell BRAIN MATRIX Platform Study forms the backbone of this programme. In the Platform Study, the aim is to develop the infrastructure to provide rapid and accurate molecular diagnosis and the infrastructure to deliver clinical trials of new therapies in the future, thereby improving clinical outcomes in brain tumours. The researchers aim to recruit 1,000 patients to the study. As gliomas occur at all ages and their specific subtype is hard to predict pre-operatively, the patient population eligible for the study is broad. A large network of clinical hubs across the UK, with expertise in managing patients with brain tumours, will be developed. Once established this infrastructure will facilitate the rapid introduction of clinical trials testing targeted therapies tailored to the genetic changes of an individual's tumour. Eligible patients will either have had, or be about to have, surgery for their tumour. As part of this study, tumour removed during the operation will be analysed to look for specific molecular changes. As with normal standard care, the tumour will be analysed by a local pathologist. A small part will be sent for review by experts and advanced molecular analysis will be undertaken to get a detailed understanding of the DNA/molecular changes within the patient's tumour. These results will be fed back to the patient's treating doctor. It is intended that this will occur within 28 days; however, it may be longer while the study becomes fully operational. If samples are available from a patient's previous surgery to their tumour, these may also be analysed. Similarly, if available, other relevant samples such as cerebrospinal fluid, collected as part of their care, may also be analysed. In addition, as technologies and analyses improve the understanding of brain tumours, the researchers may find important results at a later date. These will be fed back to the patient's doctor. Patients will also be asked to give a blood sample, which will also be analysed to look at the molecular features, including of their DNA. This is required to identify what 'new' changes have occurred in the patient's tumour. Following surgery, patients will continue with other treatment(s) as directed by their doctor. Treatment generally involves radiotherapy and chemotherapy. As is standard practice, patients will be closely monitored for signs of disease progression and the effects of the treatment given. As part of this study, information on patients' treatments and disease will be collected. Images from brain scans patients undergo, along with relevant clinical information, will also be sent to and stored by the University of Edinburgh, and where appropriate, undergo expert review by a panel of radiologists with expertise in brain tumours. If patients have further surgery, some of the tissue removed may also be analysed.

Glioma

How this trial compares with your answers

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What we know so far

Condition· Matched your search
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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: 16 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Newly diagnosed suspected WHO Grade 2-4 glioma, (as evidenced radiologically) AND suitable for a diagnostic or...
  • ✓Patients with progression with known WHO Grade 2-4 glioma (those with available frozen tumour will be prioritised...
  • ✓Valid written agreement to take part for the study.

Who cannot take part

  • ✗Primary spinal cord tumours
  • ✗Active treatment of other cancer
  • ✗safety concern to MRI
  • ✗Patients without the usual treatment imaging available
See the full criteria
Inclusion Criteria: * Newly diagnosed suspected WHO Grade 2-4 glioma, (as evidenced radiologically) AND suitable for a diagnostic or therapeutic surgical procedure resulting in a tumour sample matched to a blood sample. * Patients with progression with known WHO Grade 2-4 glioma (those with available frozen tumour will be prioritised for detailed genomic analysis). * Valid written informed consent for the study. Exclusion Criteria: * Primary spinal cord tumours * Active treatment of other malignancy * Contraindication to MRI * Patients without standard of care imaging available

Where Is This Study? (14 UK sites)

Queen Elizabeth Hospital Birmingham, University Hospitals Birmingham NHS Foundation Trust

Birmingham B15 2TH, United Kingdom

Recruiting
Site contact (verified)
Victoria WykesPrincipal Investigator

Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust

Cambridge CB2 0QQ, United Kingdom

TERMINATED
Hospital R&D contact (matched)

Stephen Kelleher

cuh.research@nhs.net01223 348490

Velindre Cancer Centre, Velindre University NHS Trust

Cardiff CF14 2TL, United Kingdom

Recruiting
Site contact (verified)
Jillian MacleanPrincipal Investigator

NHS Lothian

Edinburgh EH4 2XU, United Kingdom

ACTIVE_NOT_RECRUITING
Hospital R&D contact (matched)

Accord Office

enquiries@accord.scot0131 242 3330

Queen Elizabeth Unviersity Hospital, NHS Greater Glasgow and Clyde Health Board

Glasgow G51 4TF, United Kingdom

ACTIVE_NOT_RECRUITING
Hospital R&D contact (matched)

Radek Penar

radoslaw.penar@nhs.scotn/a

St James's University Hospital, Leeds Teaching Hospitals NHS Trust

Leeds LS9 7TF, United Kingdom

Recruiting
Site contact (verified)
Ryan MathewPrincipal Investigator

The Walton Centre, The Walton Centre NHS Foundation Trust

Liverpool L9 7LJ, United Kingdom

Recruiting
Site contact (verified)
Michael JenkinsonPrincipal Investigator

King's College Hospital, King's College Hospital NHS Foundation Trust

London SE5 9RS, United Kingdom

Recruiting
Site contact (verified)
Keyoumars AshkanPrincipal Investigator

Charing Cross Hospital, Imperial College Healthcare NHS Trust

London W6 8RF, United Kingdom

Recruiting
Site contact (verified)
Matthew WilliamsPrincipal Investigator

The Christie Hospital, The Christie NHS Foundation Trust

Manchester M20 4BX, United Kingdom

Recruiting
Site contact (verified)
Catherine McBainPrincipal Investigator

Salford Royal Hospital, Northern Care Alliance NHS Foundation Trust

Manchester M6 8HD, United Kingdom

Recruiting
Site contact (verified)
David CoopePrincipal Investigator

Freeman Hospital, The Newcastle upon Tyne Hospitals NHS Foundation Trust

Newcastle upon Tyne NE7 7DN, United Kingdom

Recruiting
Site contact (verified)
Joanne LewisPrincipal Investigator

Queen's Medical Centre, Nottingham University Hospitals NHS Trust

Nottingham NG7 2UH, United Kingdom

Recruiting
Site contact (verified)
Stuart SmithPrincipal Investigator

Churchill Hospital, Oxford University Hospitals NHS Foundation Trust

Oxford OX3 9DU, United Kingdom

Recruiting
Site contact (verified)
Meera NandhabalanPrincipal Investigator

How to Get in Touch

Rhys Mant

Sponsor contact

CONTACT

0121 414 6788 brainmatrix@trials.bham.ac.uk

Joshua Savage

Sponsor contact

CONTACT

j.savage.1@bham.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2026-04