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CLIMB: CNS Lymphoma Imaging and Molecular Biomarkers Study

Sponsor: Royal Marsden NHS Foundation Trust

NCT ID: NCT05828628

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
Not specified by the sponsor
How long the study runs
Study runs about 96 months (dates as stated)
About the drug or intervention
Not specified by the sponsor
Patient visit burden
Not specified by the sponsor

In plain English

CLIMB is a study for people with primary central nervous system (CNS) lymphoma, a cancer that affects the brain or spinal cord. The study looks at scans (imaging) and molecular markers (biomarkers) to learn more about this illness. The study is run by the Royal Marsden NHS Foundation Trust.

Who can take part

  • You are aged 18 or over.
  • You have been diagnosed with primary CNS lymphoma, based on either a scan or a tissue sample (biopsy).
  • You have not had any treatment aimed at the CNS before. Taking steroids beforehand is allowed.
  • You are able to give your own agreement (consent) to take part. If the illness affects your ability to decide, a representative can agree on your behalf, following English or Scottish law.

Who may not be able to

  • The lymphoma is also present outside the CNS (the brain and spinal cord).

What taking part involves

  • • The study involves scans (imaging) and tests looking at molecular markers (biomarkers).
  • • Any other tests or treatments involved are not stated — ask the trial team.

Time commitment: Visits, duration, and what taking part involves are not stated — ask the trial team.

Plain-English summary (AI-generated) from registry data. Not eligibility advice — only the trial team can confirm whether you can take part. Use the eligibility checker to see how your health profile matches this trial.

Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
36
Started
2023-09-18
Last checked
2024-11

Plain English Summary

What is this study?

  • • Testing a new treatment for cns lymphoma
  • • Clinical study - 36 participants
  • • A prospective imaging and translational tissue study in CNS lymphoma to enable further disease characterisation and the development of potential predictive and prognostic biomarkers

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with cns lymphoma

Where?

  • • Sutton - The Royal Marsden NHS Foundation Trust, Downs Road

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

About This Trial

A prospective imaging and translational tissue study in CNS lymphoma to enable further disease characterisation and the development of potential predictive and prognostic biomarkers.

More detail

As a single centre exploratory study, this trial will recruit patients with newly diagnosed primary CNS lymphoma and will look at the molecular aspects of the disease in the tissue collection and imaging response assessments using CCA with respect to progression free survival.

CNS Lymphoma

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

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: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓A radiological or histological diagnosis of primary CNS lymphoma.
  • ✓Have not received prior CNS directed therapy. Prior use of steroids is permitted.
  • ✓Participants aged ≥18 years old.

Who cannot take part

  • ✗\- Involvement of lymphoma outside of the CNS
See the full criteria
Inclusion Criteria: * Subjects capable of giving informed consent, or if appropriate, if subject's capacity is deemed limited due to CNS involvement, a consultee can provide consent on their behalf. Some patients with PCNSL may be incapable of providing their own consent due to the neurological effects of their disease. In these cases the patient will be classed as an incapacitated adult and a legal representative will be sought in accordance with English or Scottish law as applicable (see 7.2.1) * A radiological or histological diagnosis of primary CNS lymphoma. * Have not received prior CNS directed therapy. Prior use of steroids is permitted. * Participants aged ≥18 years old. Exclusion Criteria: \- Involvement of lymphoma outside of the CNS

Where Is This Study? (1 UK site)

The Royal Marsden NHS Foundation Trust, Downs Road

Sutton SM2 5PT, United Kingdom

Recruiting
Site contact (verified)

How to Get in Touch

GI and Lymphoma Unit

Sponsor contact

CONTACT

02086426011 GI.Trials@rmh.nhs.uk
Data sourced from ClinicalTrials.gov · Last verified: 2024-11