Phase 2 Mesothelioma Trial, Recruiting NCT05932199 Sponsor: Baylor College of Medicine Condition: Mesothelioma
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Phase 2 Mesothelioma Trial, Recruiting

NCT05932199
Recruiting Phase 2

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 have a type of cancer called malignant pleural mesothelioma (MPM) that a specialist surgeon believes may be removable with surgery, based on scans showing the cancer has not spread beyond one side of the chest
  • You are willing to undergo planned surgery to remove the tumor (one of two types of chest surgery)
  • Your mesothelioma can be any cell type (epithelial, mixed, or sarcomatoid)
  • The cancer may or may not have spread to nearby lymph nodes
  • You are over 18 years old
  • You are generally well enough to carry out light activity and care for yourself (confirm with trial site)
  • Your blood counts, liver, and kidney function are within acceptable ranges as shown by blood tests
  • If you are a woman who could become pregnant, you must have a negative pregnancy test before joining
  • You weigh more than 30 kg (about 66 lbs)
  • You are willing and able to attend all required appointments and follow the study schedule

Who may not be able to join:

  • You have previously been treated with certain immunotherapy drugs that target PD-1, PD-L1, or CTLA-4 pathways, including durvalumab
  • You have taken part in another clinical trial with an experimental drug in the last 3 months
  • You received any anti-cancer treatment less than 28 days before joining the study
  • You have certain heart rhythm abnormalities detected on a heart tracing (ECG) (confirm with trial site)
  • You have been taking immune-suppressing medications in the 28 days before starting the study (with some exceptions such as low-dose steroid inhalers or very low-dose oral steroids)
  • You have unresolved significant side effects from a previous cancer treatment (for a cancer other than MPM)
  • You previously had a serious immune-related reaction to immunotherapy
  • You have an autoimmune condition that requires strong immune-suppressing medication
  • You have a history of lung inflammation caused by the immune system, or currently have lung inflammation
  • You have a history of a condition where your immune system does not work properly from birth
  • You have had an organ transplant from another person
  • You have had a serious reaction to immunotherapy drugs in the past
  • You have a serious heart condition or other severe uncontrolled medical problem
  • You have HIV, AIDS, active hepatitis B, or another serious ongoing infection requiring treatment
  • You currently have an active infection requiring antibiotics, antifungal, or antiviral drugs (preventive antibiotics are usually acceptable)
  • You have a history of cancer spreading to the membranes around the brain or spinal cord
  • You received a live vaccine within 30 days before starting the study
  • You are pregnant, breastfeeding, or not using effective birth control (if able to have children)
  • You have brain metastases that are causing symptoms or require active treatment
  • You have uncontrolled seizures
  • You are female and of reproductive potential without a negative pregnancy test at study entry
  • No tumor tissue sample can be obtained during an initial surgical procedure (thoracoscopy)

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 27 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Robert Ripley, MD, Baylor College of Medicine

Phone: 713-798-5530

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
Phase 2
Registry
ClinicalTrials.gov
Start date
3 July 2024
Est. completion
31 May 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Recurrence-free survival of greater than 60% at one year.

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: 27 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