Actively Recruiting

Age: 18Years +
All Genders
ID05828628

A Prospective Imaging and Translational Tissue Study in CNS Lymphoma to Enable Further Disease Characterisation and the Development of Potential Predictive and Prognostic Biomarkers

Led by Royal Marsden NHS Foundation Trust · Updated on 2025-06-11

36

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating primary central nervous system (CNS) lymphoma through an observational study to better understand the disease at a molecular level. This study aims to identify potential biomarkers that could predict disease progression and outcomes by examining tissue samples and imaging data. The study is conducted at a single center and focuses on patients newly diagnosed with primary CNS lymphoma. Participants will undergo imaging assessments using Contrast Clearance Analysis (CCA) and tissue sample collection to evaluate molecular characteristics of their lymphoma. The study monitors plasma circulating tumor DNA (ctDNA) and imaging responses over a period of five years to explore links with progression-free survival. No experimental treatments are given, as this is an observational study. Throughout the study, participants will provide tissue samples and blood samples for ctDNA analysis at multiple time points, including baseline, end of treatment, and disease progression. Imaging scans using CCA will also be performed to assess disease status. Researchers will track and analyze these data over five years to gather insights into disease behavior and potential biomarkers. Participation duration extends up to five years with periodic assessments and monitoring.

CONDITIONS

Brief Title

CLIMB: CNS Lymphoma Imaging and Molecular Biomarkers Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Able to give informed consent or have a legal representative provide consent if capacity is limited due to CNS involvement
  • Radiological or histological diagnosis of primary CNS lymphoma
  • Have not received prior CNS-directed therapy (prior steroid use allowed)
  • Age 18 years or older
Not Eligible

You will not qualify if you...

  • Lymphoma involvement outside of the central nervous system

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - At diagnosis

Participants undergo imaging and tissue collection to assess disease characteristics and molecular aspects.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 5 years

Participants are monitored over time with imaging and plasma tests to evaluate disease progression and biomarker presence.

Periodic visits during follow-up

Trial Site Locations

Total: 1 location

1

The Royal Marsden NHS Foundation Trust, Downs Road

Sutton, United Kingdom, SM2 5PT

Actively Recruiting

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Research Team

G

GI and Lymphoma Unit

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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