Collection of Research Data and Samples From Patients Who Experience Immunotherapy Side Effects
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- STATUS
- Recruiting
-
- participants needed
- 240
-
- sponsor
- Alliance for Clinical Trials in Oncology
Summary
This trial collects research data and samples from patients who experience immunotherapy side effects to store for use in future research studies. Studying research data and samples from patients who experience immunotherapy side effects may help researchers better understand how to predict, prevent, and treat these side effects.
Description
PRIMARY OBJECTIVES:
To establish a national biorepository including biospecimen and clinical data collections
from patients treated with immuno-oncology (IO) therapeutics who experience one or more
serious (grade 3-5) immune-related adverse events (irAEs), rare infections or
hyperprogression (acceleration of
- OUTLINE
Patients undergo collection of tissue and blood samples (and optional stool samples from
patients experiencing
Details
| Condition | Cancer |
|---|---|
| Age | 100years or below |
| Treatment | Biospecimen Collection, Medical Chart Review |
| Clinical Study Identifier | NCT04242095 |
| Sponsor | Alliance for Clinical Trials in Oncology |
| Last Modified on | 19 February 2024 |
How to participate?
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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