Durvalumab and Tremelimumab for Mesothelioma

This study is testing two different treatment approaches for people with mesothelioma that can potentially be removed by surgery. One group will receive a combination of chemotherapy (cisplatin or carboplatin and pemetrexed) along with two immunotherapy drugs, durvalumab and tremelimumab. The other group will receive only the immunotherapy drugs, durvalumab and tremelimumab. The main goal is to see if either of these treatments can improve how long patients live without their cancer returning after surgery, aiming for more than 60% of patients to be recurrence-free at one year. The study plans to enroll 52 participants and is currently unclear on its recruitment status. You may be eligible if you are 18 or older and have mesothelioma that a surgeon believes can be removed.

Study design
This is a randomized Phase Ib/IIa study with two groups, enrolling a total of 52 participants. It compares two different treatment combinations.
What's involved
Participants will receive treatment for 3 cycles before surgery, and then continue with durvalumab for up to 12 months after surgery. Tremelimumab will be given up to cycle 5.
Compensation
Not stated in the trial record.
Follow-up
The primary endpoint measures recurrence-free survival at one year after treatment.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT05932199

Neoadjuvant Durvalumab and Tremelimumab With and Without Chemotherapy for Mesothelioma

Recruiting
PHASE1Ages 18+InterventionalTreatment
Baylor College of Medicine
~52 participants
Updated 2025-09-25 on ClinicalTrials.gov
What's tested:Durvalumab / tremelimumabPlatinum cisplatin or carboplatin and pemetrexed chemotherapy plus durvalumab/tremelimumab

At a glance

Recruiting sites
1 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Recurrence-free survival of greater than 60% at one year.
Measured over Recurrence-free survival of greater than 60% at one year.
Mesothelioma

NCT05932199

Where you'd take part

This study runs at 2 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Baylor St Lukes

    Houston, Texasstudy coordinator listed

    Recruiting

  • Duke Cancer Institute

    Durham, North Carolinastudy coordinator listed

    Not yet recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Robert Ripley, MD · PRINCIPAL_INVESTIGATOR · Baylor College of Medicine

Opens a ready-to-send draft in your own email app — review before sending.

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

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