Randomized, Double-blind Study Comparing Tremelimumab to Placebo in Subjects With Unresectable Malignant Mesothelioma

Running, not enrolling · Phase 2 · Has a placebo group

Conditions studied: Unresectable Pleural or Peritoneal Malignant Mesothelioma

In brief

This is a Phase 2b, randomized, double-blind, parallel-group study. Subjects with unresectable pleural or peritoneal malignant mesothelioma will be randomized in a 2:1 ratio to receive either tremelimumab or placebo. Approximately 564 subjects will be enrolled at study centers in multiple countries. The study consists of a screening period, a treatment period, a 90-day follow-up period for safety, and a long-term survival follow-up period.

Key facts

Study ID

NCT01843374

Run by

MedImmune LLC

People needed

571

Starts

2013-05-17

Expected to finish

2027-05-31

Last updated by the study team

2026-07-27

Who can join

Age: 18 and older, up to 99. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Histologically and/or cytologically confirmed pleural or peritoneal malignant mesothelioma;
• Disease not amenable to curative surgery;
• Age 18 and over at the time of consent;
• ECOG Performance status 0-1;
• Progressed after previous receipt of 1-2 prior systemic treatments for advanced disease that included a first-line pemetrexed (or anti-folate)-based regimen in combination with platinum agent.
• Recovered from all toxicities associated with prior treatment, to acceptable baseline status, or a NCI CTCAE Grade of 0 or 1, except for toxicities not considered a safety risk,
• Measurable diseaseby modified RECIST for pleural mesothelioma or RECIST v1.1 for peritoneal mesothelioma;
• Adequate bone marrow, hepatic, and renal function determined within 14 days prior to randomization defined as:
• Negative screening test results for human immunodeficiency virus (HIV), hepatitis A, B and C.
• Written informed consent and any locally required authorization (eg, HIPAA in the USA, EU Data Privacy Directive authorization in the EU) obtained from the subject/legal representative prior to performing any protocol- related procedures, including screening evaluations;
• Females of childbearing potential who are sexually active with a nonsterilized male partner must use a highly effective method of contraception for 28 days prior to the first dose of investigational product, and must agree to continue using such precautions for 6 months after the final dose of investigational product; cessation of contraception after this point should be discussed with a responsible physician.
• Nonsterilized males who are sexually active with a female partner of childbearing potential must use a highly effective method of contraception from Days 1 through 90 post last dose. In addition, they must refrain from sperm donation for 90 days after the final dose of investigational product.

You may not qualify if…

• Subjects who failed more than 2 prior systemic treatment regimens for advanced malignant mesothelioma;
• Received any prior mAb against CTLA-4, programmed cell death 1 (PD1) or programmed cell death 1 ligand 1 (PD-L1);
• History of chronic inflammatory or autoimmune disease with symptomatic disease within the last 3 years prior to randomization.
• Active, untreated central nervous system (CNS) metastasis
• Any serious uncontrolled medical disorder or active infection that would impair the subject's ability to receive investigational product;
• History of other malignancy unless the subject has been disease-free for at least 3 years;
• Pregnant or breast feeding at time of consent;
• Any condition that would prohibit the understanding or rendering of information and consent and compliance with the requirements of this protocol;
• Active or history of diverticulitis;
• Active or history of inflammatory bowel disease, irritable bowel disease, celiac disease or other serious gastrointestinal chronic conditions associated with diarrhea. Active or history of systemic lupus erythematosus or granulomatosis with polyangiitis;
• History of sarcoidosis syndrome;
• Currently receiving systemic corticosteroids or other immunosuppressive medications or has a medical condition that requires the chronic use of corticosteroids.
• Subjects should not be vaccinated with live attenuated vaccines within one month prior to starting tremelimumab treatment;
• The last dose of prior chemotherapy or radiation therapy was received less than 2 weeks prior to randomization;
• Any unresolved toxicity NCI CTCAE Grade ≥ 2 from previous anticancer therapy with the exception of vitiligo and alopecia;
• Any condition that, in the opinion of the investigator, would interfere with evaluation of the investigational product or interpretation of subject safety or study results;
• Concurrent enrollment in another clinical study or receipt of an investigational product within the last 4 weeks
• Employees of the study site directly involved with the conduct of the study, or immediate family members of any such individuals;
• Subjects with a history of hypersensitivity to compounds of similar biologic composition to tremelimumab or any constituent of the product.

Where it is running

• Research Site — La Jolla, California, United States
• Research Site — Los Angeles, California, United States
• Research Site — San Francisco, California, United States
• Research Site — Santa Monica, California, United States
• Research Site — New Haven, Connecticut, United States
• Research Site — Newark, Delaware, United States
• Research Site — Tampa, Florida, United States
• Research Site — Augusta, Georgia, United States
• Research Site — Chicago, Illinois, United States
• Research Site — Peoria, Illinois, United States
• Research Site — Baltimore, Maryland, United States
• Research Site — Baltimore, Maryland, United States
• Research Site — Minneapolis, Minnesota, United States
• Research Site — New York, New York, United States
• Research Site — Rochester, New York, United States
• Research Site — Durham, North Carolina, United States
• Research Site — Canton, Ohio, United States
• Research Site — Philadelphia, Pennsylvania, United States
• Research Site — Dallas, Texas, United States
• Research Site — Houston, Texas, United States
• Research Site — Adelaide, Australia
• Research Site — Auchenflower, Australia
• Research Site — Box Hill, Australia
• Research Site — Chermside, Australia
• Research Site — Scottsdale, Arizona, United States

Full record on ClinicalTrials.gov

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