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Evaluating Informatics-assisted Immune-related Adverse Event Detection to Improve Registration Onto a Biorepository

RecruitingPhase 1, Phase 2Ages any - anyAllBrigham and Women's Hospital
NCT06789601 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

Immunotherapies have improved cancer outcomes, but have a unique profile of immune-related adverse events (irAEs). Biorepositories have been established to collect data and samples to help improve our understanding of irAEs, however identifying patients who are eligible for these biorepositories in a timely fashion can be challenging. The goal of this study is to determine if an informatics system for automated irAE detection can improve registration to a prospective irAE biorepository (NCT04242095). The informatics system automatically "reads" participants' electronic health records (EHRs) and determines whether that patient may be experiencing an irAE. The main questions it aims to answer are: * Is it feasible to implement an informatics system for daily analysis of EHR data to detect irAEs? * Does the automated irAE detection system improve registration rates to an irAE biorepository

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📋 Eligibility rules (as published)
Inclusion Criteria: * Received or receiving a regimen containing one or more immuno-oncology therapeutics
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What it tests

  • Informatics system for eligibility monitoring
  • Standard eligibility monitoring
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Where

2 sites
Brigham and Women's Hospital
Boston, United States
Dana-Farber Cancer Institute
Boston, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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