RecruitingNCT04680377
Using Microbiome to Predict Durvalumab Toxicity in Post- Concurrent Chemoradiation Therapy (CCRT) NSCLC Patients
Using Microbiome to Predict Durvalumab Toxicity in Post-CCRT NSCLC Patients (Microdurva)
Sponsor
Jun Zhang, MD, PhD
Enrollment
44 participants
Start Date
Apr 12, 2021
Study Type
OBSERVATIONAL
Conditions
Summary
This phase IV study is hoping to determine if examining the microbiome in non-small cell lung cancer participants who will receive durvalumab can predict treatment toxicity.
Eligibility
Min Age: 18 Years
Plain Language Summary
Simplified for easier understanding
This study is exploring whether the mix of bacteria living in your gut (your microbiome) can predict which lung cancer patients will have serious side effects from a drug called durvalumab — an immunotherapy given after chemotherapy and radiation for non-small cell lung cancer (NSCLC).
**You may be eligible if...**
- You are 18 or older
- You have non-small cell lung cancer treated with at least two cycles of platinum-based chemotherapy plus radiation (54–66 Gy)
- You have a life expectancy of at least 12 weeks
- You are in good physical condition (ECOG 0 or 1)
- You are able to follow study visits and procedures
**You may NOT be eligible if...**
- You have not had the required prior chemotherapy and radiation
- Your overall health does not meet the study's organ function requirements
- You are unable or unwilling to consent and comply with the study
Talk to your doctor to see if this trial is right for you.
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Locations(2)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT04680377
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