Using Microbiome to Predict Durvalumab Toxicity in Post- Concurrent Chemoradiation Therapy (CCRT) NSCLC Patients

NCT04680377 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 44

Last updated 2024-05-08

No results posted yet for this study

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.

Conditions

  • NSCLC, Stage III
  • Locally Advanced Lung Carcinoma

Sponsors & Collaborators

  • Rhode Island Hospital

    collaborator OTHER
  • Jun Zhang, MD, PhD

    lead OTHER

Principal Investigators

  • Jun Zhang, MD, PhD · The University of Kansas Cancer Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-04-12
Primary Completion
2025-12-31
Completion
2026-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04680377 on ClinicalTrials.gov