Analysis of Biopsy Specimens to Study Responses to PD-1 or PD-L1 Therapies
Withdrawn before enrolling
Conditions studied: Non Small Cell Lung Cancer
In brief
The purpose of this study is to attempt to obtain an on-treatment biopsy in participants with non-small cell lung cancer who are receiving standard treatment with a drug that targets the PD-1 or PD-L1 protein.
Key facts
- Study ID
- NCT03877250
- Run by
- Memorial Sloan Kettering Cancer Center
- People needed
- 0
- Starts
- 2019-03-08
- Expected to finish
- 2020-08-26
- Last updated by the study team
- 2025-05-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Pathologically confirmed newly diagnosed or recurrent advanced Non Small Cell Lung Cancer/NSCLC that is PI-L1 high by immunohistochemistry (PD-L1 >/= 50%)
- Intended treatment with a PD-(L)1 inhibitor
- Age >/= 18 years
- Karnofsky Performance Status >/= 70% and medically fit to undergo a biopsy procedure
You may not qualify if…
- Any medical condition or any sites of disease that would preclude a biopsy
- Pregnant or breastfeeding women
- Cognitively impairment affecting ability to understand and provide informed consent
- Prior PD-(L)1 blockade treatment
- Chemotherapy within 6 months prior to enrollment
Where it is running
- Memoral Sloan Kettering Basking Ridge (Consent and Follow up) — Basking Ridge, New Jersey, United States
- Memoral Sloan Kettering Monmouth (Consent and Follow up) — Middletown, New Jersey, United States
- Memorial Sloan Kettering Bergen (Consent and Follow up) — Montvale, New Jersey, United States
- Memorial Sloan Kettering Cancer Center @ Suffolk (Consent Only) — Commack, New York, United States
- Memoral Sloan Kettering Westchester (Consent & Follow Up) — Harrison, New York, United States
- Memorial Sloan - Kettering Cancer Center (Consent and follow-up) — New York, New York, United States
Full record on ClinicalTrials.gov
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