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Immune Checkpoint Inhibitor Toxicity Risk Prediction in Solid Tumors
NCT04871542 · View on ClinicalTrials.gov ↗
Study Summary
This study examines how certain risk factors (such as age, gender, other medical conditions, and the type of immunotherapy used to treat the cancer) affect whether a patient with a malignant solid tumor will develop mild or serious side effects from the immunotherapy medications. Immunotherapy is the type of treatment that helps the body's immune system fight cancer. In the future, this information may help doctors make better decisions about cancer treatments.
Conditions Studied
Interventions
- PROCEDURE Biospecimen Collection
- OTHER Questionnaire Administration
Study Locations (6)
Iowa
- Mary Greeley Medical Center — Ames
- McFarland Clinic PC - Ames — Ames
- McFarland Clinic PC-Boone — Boone
- McFarland Clinic PC-Trinity Cancer Center — Fort Dodge
- McFarland Clinic PC-Jefferson — Jefferson
- McFarland Clinic PC-Marshalltown — Marshalltown
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2,062 participants |
| Start Date | 2021-09-13 |
| Est. Completion | 2028-03-14 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04871542
The ClinicalTrials.gov registry entry for NCT04871542 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 2,062 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is SWOG Cancer Research Network, which has 212 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Malignant Solid Neoplasm appearing as the primary indexed condition, and to 2 interventions — of which Biospecimen Collection is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04871542 reports 6 study locations spanning 1 distinct geographic area — top geographies include Iowa. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04871542 about?
NCT04871542 is a clinical study titled "Immune Checkpoint Inhibitor Toxicity Risk Prediction in Solid Tumors". This study examines how certain risk factors (such as age, gender, other medical conditions, and the type of immunotherapy used to treat the cancer) affect whether a patient with a malignant solid tumor will develop mild or serious side effects from the immunotherapy medications. Immunotherapy is th...
What is the current status of trial NCT04871542?
This trial is currently recruiting. The enrollment target is 2,062 participants. The study started on 2021-09-13. Estimated completion is 2028-03-14.
What conditions does trial NCT04871542 study?
This clinical trial studies the following conditions: Malignant Solid Neoplasm. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04871542?
The interventions under investigation include: Biospecimen Collection (PROCEDURE), Questionnaire Administration (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04871542?
This trial is sponsored by SWOG Cancer Research Network, which has 212 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04871542 being conducted?
This trial has 6 study locations across Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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