Olaparib in Patients With HRD Malignant Mesothelioma

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Chicago

About this trial

In this study, researchers will give olaparib (a drug) to mesothelioma patients who have specific changes in their DNA (known as gene mutations). Researchers will give this drug to each patient on the study to find out if it will help the patient's tumor shrink or stop growing.

Eligibility criteria

Qualifiers

Must have a medical diagnosis of malignant mesothelioma that has been confirmed by a physician.

Participant must be able to sign a consent form stating that they choose (of their own free will) to participate in the study and agree to follow the study requirements and restrictions that are listed in the consent form.

Must be willing to sign and date consent form before any mandatory study-specific procedures, sample collecting and tests.

Willing to experience genetic testing to determine study eligibility. Must be willing to genetically test tumor and normal body cells.

Disqualifiers

Any evidence of uncontrollable illness that the physician leading this study deems undesirable for the patient to participate in the trial.

Other malignancy (tumor/cancer) unless it has been treated with no evidence of disease for 3 or more years except: adequately treated non-melanoma skin cancer, curatively treated in situ cancer of the cervix, ductal carcinoma in situ (DCIS), Stage 1, grade 1 endometrial carcinoma.

Patients with BAP1 tumor predisposition syndrome will be included in the trial. These patients may be eligible if they have a history of syndrome-related cancers, provided they completed their surgery and chemotherapy more than three years prior to registration, and the patient remains free of disease that continues to re-occur or spread to other parts of the body.

Patients with cancer that does not respond to platinum chemotherapy drugs (known as platinum-resistant disease), defined as disease progression during or within 3 months of receiving chemotherapy.

Trial design

Treatments tested in this trial

  • Olaparib

Treatment groups

56 Participants
are divided into 1 treatment group

Sponsors and collaborators

University of Chicago

Lead sponsor

AstraZeneca

Collaborator