Mesothelioma Trial, Recruiting NCT07126509 Sponsor: University of Chicago Condition: Mesothelioma
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Mesothelioma Trial, Recruiting

NCT07126509
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:

  • You must have a confirmed diagnosis of a specific type of mesothelioma (called "epithelioid" subtype) affecting the lining of the lung, confirmed through a surgical biopsy procedure.
  • The cancer must be located only on one side of the chest.
  • Your cancer must be considered either unable to be fully removed by surgery, or only possibly removable with complex surgery, based on CT or MRI scans showing it has grown into nearby structures or is very large.
  • You must have already completed at least 6 weeks of chemotherapy or immunotherapy treatment (such as certain drug combinations including platinum-based chemotherapy, pemetrexed, pembrolizumab, bevacizumab, or ipilimumab/nivolumab), with no serious unresolved side effects.
  • You must be 18 years old or older.
  • You must be generally healthy and active enough to carry out daily activities with no more than minor limitations (confirm with trial site).
  • Your blood, liver, and kidney test results must be within acceptable ranges as measured by specific blood tests.
  • If you have HIV, you must be on effective treatment with an undetectable level of the virus in the past 6 months.
  • If you have a history of hepatitis B, the virus must be at undetectable levels while on treatment.
  • If you have a history of hepatitis C, you must have been successfully treated and cured, or currently on treatment with undetectable virus levels.
  • If you have a history of heart disease or have received treatments that can affect the heart, your heart function must meet a minimum standard as assessed by your doctor (confirm with trial site).
  • Your case must have been reviewed by a team of specialists including surgeons, radiologists, pathologists, cancer doctors, and palliative care doctors.
  • You must be enrolled or willing to enroll in a related tissue research study at the University of Chicago.
  • You must be willing and able to sign an informed consent form agreeing to take part in the trial.

Who may not be able to join:

  • People who have a different subtype of mesothelioma (called "biphasic" or "sarcomatoid") cannot join.
  • People whose cancer has spread to other parts of the body, or into the abdominal (belly) area, cannot join.
  • People whose cancer continued to grow or spread during or after their initial treatment cannot join.
  • People whose lung function test results fall below certain thresholds, suggesting the lungs are not strong enough for surgery, cannot join (confirm with trial site).
  • People who are currently participating in another clinical trial involving an experimental treatment cannot join.
  • People who have another illness that is not well controlled cannot join.
  • People who have had another type of cancer that was active within the past 2 years cannot join, unless it was an easily treatable skin cancer, early-stage bladder cancer, or a very early-stage cancer of the prostate, cervix, breast, or thyroid that has been successfully treated.

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

Principal Investigator: Darren Bryan, MD, University of Chicago

Phone: 1-855-702-8222

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
2 December 2025
Est. completion
1 December 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Disease-related Symptom Burden 3 Months After Partial Pleurectomy (Surgery)

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