Can we predict dangerous side effects of immunotherapy?
NCT ID NCT07527585
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aims to find biological markers that can predict immune-related side effects in cancer patients receiving immune checkpoint inhibitor therapy. Researchers will collect data from 440 participants to build a model that forecasts these adverse events. The goal is to improve safety and personalize treatment for patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 440 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2032
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
patients with malignancies undergoing immunotherapy
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age \>18 years; 2. Karnofsky Performance Status (KPS) \>60; 3. Expected to receive at least one cycle of immune checkpoint inhibitor therapy; 4. Expected survival \>6 months. Exclusion Criteria: 1. Prior treatment with immune checkpoint inhibitors; 2. Active autoimmune diseases (including systemic lupus erythematosus, inflammatory bowel disease, rheumatoid arthritis, myasthenia gravis, scleroderma, etc.); 3. Use of systemic immunosuppressive agents within 14 days prior to enrollment (prednisone \>10 mg/day or equivalent); 4. Inability to provide biological samples.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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