Assess Diversity of Gut Microbiome in Met NSCLC in Correlation to Tx & Adverse Effects
Recruiting · NCT06221800 · Observational (researchers observe without assigning treatment)
View the official record on ClinicalTrials.gov →Interventions studied
Microbiome
What this trial is about
This is a pilot study collecting data on the diversity and composition of gut microbiomes in subjects with advanced/metastatic Non-Small Cell Lung Cancer (NSCLC) while receiving treatment for NSCLC.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- 1\. Advanced/Metastatic non-small cell lung cancer NSCLC patients.
- 2\. The patient himself/herself must be 18 years of age on day of signing informed consent.
- 3\. The subject has signed the informed consent form.
- 4\. The patient must be eligible to receive FDA approved and non-approved PD1 inhibitors (i.e. pembrolizumab, nivolumab) or PDL1 inhibitor (i.e. atezolizumab, durvalumab) either single agent or as combination therapy with chemotherapy, or be eligible to receive FDA approved and non-approved tyrosine kinase inhibitors.
- 5\. The subject will be registered upon submission of the samples. When submitted on separate dates, the submission occurring later will be considered the date of registration
Exclusion criteria
- 1\. Those subjects who are determined clinically unstable of the participation of this study as determined by the PI or treating physician will be excluded and asked to focus on their treatment.
Where it is running
1 location listed across 1 US state.
- Chao Family Comprehensive Cancer Center University of California, Irvine - Orange, California, United States