Mesothelioma Trial, Recruiting NCT05628376 Sponsor: University College, London Condition: Mesothelioma
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Mesothelioma Trial, Recruiting

NCT05628376
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

All groups:

  • You must be willing and able to give written consent to take part
  • You must agree to attend follow-up appointments every 3 months for the first 2 years, then every 6 months after that
  • You must be able to attend follow-up at a participating TRACERx EVO clinic

Group A (early-stage lung cancer):

  • You are 18 years old or over and have been diagnosed with early-stage non-small cell lung cancer (NSCLC, stages I to IIIB) and are able to have surgery to remove the tumour
  • Your lung cancer has been confirmed by a tissue test, or there is a strong suspicion of cancer on a scan that means surgery is needed
  • Your planned surgery follows standard medical guidelines for lung cancer operations
  • If you are having surgery without any treatment beforehand, your tumour must be at least 15mm in size so that two separate samples can be taken from it
  • If you are receiving treatment before surgery (such as chemotherapy), at least one tissue sample must be available from a biopsy or surgery
  • You are considered well enough to have surgery or pre-surgery treatment if needed
  • Your general health and ability to carry out daily activities falls within an acceptable range (performance status 0 to 2 — confirm with trial site)

Group B (advanced or spread lung cancer):

  • You are 18 years old or over and have been diagnosed with advanced or metastatic non-small cell lung cancer (NSCLC, stage IIIB or above, or stage IV)
  • At least one tissue sample is available from your biopsy or surgery
  • You are considered well enough to receive cancer treatment
  • Your general health and ability to carry out daily activities falls within an acceptable range (performance status 0 to 2 — confirm with trial site)

Group C (small cell lung cancer or pleural mesothelioma):

  • You are 18 years old or over and have been diagnosed with small cell lung cancer (SCLC) or pleural mesothelioma (a cancer affecting the lining of the lungs) at any stage
  • At least one tissue sample is available from your biopsy or surgery
  • You are considered well enough to receive cancer treatment
  • Your general health and ability to carry out daily activities falls within an acceptable range (performance status 0 to 2 — confirm with trial site)

Who may not be able to join:

All groups:

  • You currently have another type of cancer that is active or being treated (including with hormone therapy)
  • You have been diagnosed with or had a recurrence of another cancer within the past 3 years (exceptions include certain skin cancers, early-stage melanoma, and cervical cancer in situ — confirm with trial site)
  • You have a psychological condition that would prevent you from giving informed consent
  • After surgery or biopsy, it turns out your diagnosis is something other than NSCLC, SCLC, or pleural mesothelioma
  • You have a confirmed diagnosis of certain serious infections such as HIV, Hepatitis B, Hepatitis C, syphilis, tuberculosis, or Creutzfeldt-Jakob disease — unless your case is of special scientific interest and has been agreed in advance with the research team (confirm with trial site)
  • You have other health conditions that make participation unsafe (confirm with trial site)

Group A only:

  • The surgeon was unable to fully remove the tumour, or not enough lymph node samples were taken during surgery
  • It is unlikely that two separate tumour samples can be collected (for those not having pre-surgery treatment), based on scans taken before the operation
  • After surgery, it is found that your cancer was at a very early, non-invasive stage — you would be withdrawn from the study, though samples already collected would still be used

Groups B and C only:

  • There is not enough tissue available from at least one biopsy sample

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 02031085363

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
20 October 2023
Est. completion
20 October 2030

Where this trial is recruiting

🇬🇧 United Kingdom

Primary endpoints

Disease Free Survival; Progression Free Survival; Overall Survival

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov