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Search / Trial NCT06097728

MEDI5752 in Combination With Carboplatin Plus Pemetrexed in Unresectable Pleural Mesothelioma

Launched by ASTRAZENECA · Oct 18, 2023

Trial Information

Current as of August 26, 2025

Recruiting

Keywords

Mesothelioma Pleural Mesothelioma Unresectable Pleural Mesothelioma Advanced Pleural Mesothelioma

ClinConnect Summary

This clinical trial is studying a new treatment for patients with unresectable pleural mesothelioma, a type of cancer that affects the lining of the lungs and cannot be removed with surgery. Researchers want to see how well a combination of a new drug called Volrustomig (MEDI5752) along with two chemotherapy drugs, Carboplatin and Pemetrexed, works compared to other standard treatments. This is a Phase 3 trial, meaning it is one of the final steps in testing the treatment's effectiveness and safety before it can be approved for general use.

To participate in this trial, you need to be at least 18 years old and have a confirmed diagnosis of pleural mesothelioma that cannot be surgically removed. Other requirements include having measurable disease and being in good overall health, as assessed by your doctor. If you join the trial, you will receive either the new treatment combination or one of the standard treatments chosen by your doctor. This trial is currently recruiting participants, and it is important to discuss with your healthcare team if this study might be right for you.

Gender

ALL

Eligibility criteria

  • Key Inclusion Criteria:
  • Participant must be ≥ 18 years at the time of screening
  • Histologically proven diagnosis of pleural mesothelioma with known histology (epithelioid vs. non-epithelioid)
  • Advanced unresectable disease that cannot be treated with curative surgery (with or without chemotherapy)
  • WHO/ECOG performance status of 0 or 1 with no deterioration (that is, ECOG PS\>1) over the previous 2 weeks prior to day of first dosing
  • Has measurable disease per modified RECIST1.1
  • Has adequate bone marrow reserve and organ function at baseline
  • Key Exclusion Criteria:
  • As judged by the investigator, any condition that would interfere with evaluation of the investigational product or interpretation of participant safety or study results.
  • Active or prior documented autoimmune or inflammatory disorders
  • History of another primary malignancy with exceptions.
  • Uncontrolled intercurrent illness
  • Tuberculosis, hepatitis B (HBV) or hepatitis C (HCV), human immunodeficiency virus (HIV) infection that is not well controlled
  • Any concurrent chemotherapy, radiotherapy, investigational, biologic, or hormonal therapy for cancer treatment
  • Untreated or progressive CNS metastatic disease

About Astrazeneca

AstraZeneca is a global biopharmaceutical company dedicated to the discovery, development, and commercialization of innovative medicines across various therapeutic areas, including oncology, cardiovascular, respiratory, and autoimmune diseases. With a strong commitment to scientific research and patient-centric solutions, AstraZeneca leverages cutting-edge technology and a robust pipeline to address unmet medical needs. The company collaborates with healthcare professionals, academic institutions, and other organizations to advance clinical trials and deliver transformative therapies, aiming to improve health outcomes and enhance the quality of life for patients worldwide.

Locations

Rochester, Minnesota, United States

Houston, Texas, United States

Cleveland, Ohio, United States

Fairfax, Virginia, United States

Valhalla, New York, United States

Gent, , Belgium

Hasselt, , Belgium

Barretos, , Brazil

Porto Alegre, , Brazil

Varese, , Italy

Oviedo, , Spain

Aurora, Colorado, United States

Portland, Oregon, United States

Atlanta, Georgia, United States

Chicago, Illinois, United States

Columbus, Ohio, United States

Kiel, , Germany

Cleveland, Ohio, United States

Portland, Oregon, United States

Leuven, , Belgium

Edmonton, Alberta, Canada

Padova, , Italy

Warszawa, , Poland

Madrid, , Spain

Antwerpen, , Belgium

Philadelphia, Pennsylvania, United States

Lille, , France

Strasbourg, , France

Toulouse, , France

Essen, , Germany

Bari, , Italy

Rotterdam, , Netherlands

Basel, , Switzerland

Bydgoszcz, , Poland

Saint Louis, Missouri, United States

Hamilton, Ontario, Canada

Saint Herblain, , France

St. Gallen, , Switzerland

Leeds, , United Kingdom

Orbassano, , Italy

Atlanta, Georgia, United States

Duarte, California, United States

Bochum, , Germany

Lørenskog, , Norway

Middlesborough, , United Kingdom

Melbourne, , Australia

Cambridge, , United Kingdom

Leicester, , United Kingdom

London, , United Kingdom

Ottawa, Ontario, Canada

Taichung, , Taiwan

Berlin, , Germany

Heidelberg, , Germany

Barcelona, , Spain

Jacksonville, Florida, United States

Sint Niklaas, , Belgium

Regensburg, , Germany

Santa Rosa, California, United States

São Paulo, , Brazil

Beijing, , China

Chongqing, , China

Shanghai, , China

Grosshansdorf, , Germany

Olsztyn, , Poland

Baltimore, Maryland, United States

Rozzano, , Italy

Bern, , Switzerland

Commack, New York, United States

London, Ontario, Canada

Kitakyushu Shi, , Japan

Taipei, , Taiwan

Parma, , Italy

Pretoria, , South Africa

Manchester, , United Kingdom

Portsmouth, , United Kingdom

Milan, , Italy

Monza, , Italy

Matsuyama Shi, , Japan

Clayton, , Australia

Parktown, , South Africa

Kaohsiung, , Taiwan

Tokyo, , Japan

Shandong, , China

Alessandria, , Italy

Montpellier, , France

Changchun, , China

Chengdu, , China

Kunming, , China

Taiyuan, , China

Xi'an, , China

Lyon, , France

Hamburg, , Germany

Guangzhou, , China

Nishinomiya Shi, , Japan

Cape Town, , South Africa

Seoul, , Korea, Republic Of

Gauting, , Germany

Copenhagen, , Denmark

Kraaifontein, , South Africa

Phoenix, Arizona, United States

Rouen, , France

Montréal, Quebec, Canada

Quebec, , Canada

Nanchang, , China

Cheongju Si, , Korea, Republic Of

Changsha, , China

Qingdao, , China

Sao Paulo, , Brazil

Aarhus N, , Denmark

Middlesbrough, , United Kingdom

Brest, , France

Nedlands, , Australia

Chermside, , Australia

Le Mans Cedex, , France

Bergamo, , Italy

Eindhoven, , Netherlands

Hangzhou, , China

Wuhan, , China

Zhengzhou, , China

Kitaadachi Gun, , Japan

Taoyuan, , Taiwan

Ankara, , Turkey

Izmir, , Turkey

East Brunswick, New Jersey, United States

Paris, , France

Bern, , Switzerland

Creteil Cedex, , France

Anderlecht, , Belgium

Tainan City, , Taiwan

Ube Shi, , Japan

Tianjin, , China

Ulsan, , Korea, Republic Of

Westmead, , Australia

Rzeszów, , Poland

Amanzimtoti, , South Africa

Hiroshima Shi, , Japan

Okayama Shi, , Japan

Poznań, , Poland

Harbin, , China

Barakaldo, , Spain

Toronto, Ontario, Canada

Osakasayama Shi, , Japan

Newcastle Upon Tyne, , United Kingdom

Köln, , Germany

Nagoya Shi, , Japan

Santo Andre, , Brazil

Montreal, Quebec, Canada

Lanzhou, , China

Taunton, , United Kingdom

Paris Cedex 18, , France

Fortaleza, , Brazil

Johannesburg, , South Africa

Amagasaki Shi, , Japan

Essen, , Germany

Marseille Cedex 20, , France

Diyarbakir, , Turkey

Adana, , Turkey

Georgsmarienhuette, , Germany

Oslo, , Norway

Fribourg, , Switzerland

Shenyang, , China

Ningbo, , China

Amsterdam, , Netherlands

Rio De Janeiro, , Brazil

Santa Rosa, California, United States

Montreal, Quebec, Canada

Bystra, , Poland

Taiyuan, , China

Joao Pessoa, , Brazil

Münster, , Germany

Cambridge, , United Kingdom

Baden, , Switzerland

Independence, Ohio, United States

Muenster, , Germany

Cardiff, Wales, , United Kingdom

Saint Louis, Missouri, United States

Polokwane, , South Africa

Kimberly, , South Africa

Tianjin, , China

Hakodate Shi, , Japan

Patients applied

0 patients applied

Trial Officials

Marjorie G Zauderer, MD

Principal Investigator

Memorial Slone Kettering (MSK) Cancer Centre

Arnaud Scherpereel, MD

Principal Investigator

Lille University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported