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NCT07561190Recruiting

Multidimensional Omics Analysis in Malignant Pleural Mesothelioma

Multidimensional Omics and Functional Approaches to Improve Immunotherapy Efficacy in Malignant Pleural Mesothelioma

Source: ClinicalTrials.gov · Last updated 1 May 2026

Brief summary (registry, in English)

Malignant pleural mesothelioma (MPM) is a rare and incurable cancer. Most patients are diagnosed with unresectable disease for which treatment options are limited. The lack of prognostic biomarkers further complicates the decision-making. Recently, the introduction of immune checkpoint inhibitors (ICIs) has marked a shift but has failed to produce significant benefits for a large proportion of patients. Maximizing the efficiency of ICIs and developing new protocols to improve drug efficacy is the best possible strategy for improving the life expectancy and quality of life of patients with MPM. This study aims to characterize the organization of the immune system infiltrating mesothelioma and the dynamics of its interaction with the tumor. The rationale is that deciphering this complexity will help improve our understanding of the mechanisms underlying this disease and provide a new tool to optimize the use of ICIs in these patients.

Status (registry)
Recruiting
Study type
Observational
Enrollment
300 (estimated)
First submitted
16 Apr 2026
Start date
30 Aug 2024
Primary completion date
30 Aug 2024
Lead sponsor
Azienda USL Reggio Emilia - IRCCS
NCT number
NCT07561190

What you commit to

  • Study type: Observational
  • Planned participants: 300
  • From 30 Aug 2024 to the primary completion date, 30 Aug 2024
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Active current infection
  • Autoimmune disease

Age

  • Women in childbearing age not able to exclude pregnancy

Who the study is looking for

  • Participant is willing and able to give informed consent for participation in the study
  • Aged \> 18 years
  • Patients with histologically confirmed diagnosis of MPM
  • Availability of biological material
  • Clinical indicatio of eligibility for HITOCH protocol (only for C3 cohort)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Azienda Ospedaliera Universitaria Policlinico Rodolico San Marco di Catania
Coordinator of this site? Confirm its status
CataniaItalyRecruiting
Azienda Ospedaliera Universitaria Luigi Vanvitelli, Napoli
Coordinator of this site? Confirm its status
NaplesItalyRecruiting
Azienda USL IRCCS di Reggio Emilia
Coordinator of this site? Confirm its status
Reggio EmiliaItalyRecruiting
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Coordinator of this site? Confirm its status
RomaItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.