ConditionNon-Small Cell Lung Cancer (NSCLC), Small-Cell Lung Cancer (SCLC)
Official TitleA Multicenter, Low-Interventional Study to Evaluate the Feasibility of a Prospective Clinicogenomic Program
Study Summary
The main purpose of this study is to evaluate the feasibility of a scalable, prospective
research program for participants with metastatic non-small cell lung cancer (mNSCLC) or
extensive-stage small-cell lung cancer (ES-SCLC) planning to start standard-of-care (SOC)
systemic anti-cancer treatment. The study will also examine ctDNA status over the course of
treatment as a predictor of response to therapy.
Eligibility Criteria
Gender
All
Age
≥18 Years
Healthy Volunteers
No
Inclusion Criteria
Documented diagnosis of mNSCLC or ES-SCLC
Planned initiation of SOC systemic anti-cancer treatment
Front-Line Immunotherapy Cohort: Received front-line treatment of an immune blockade therapy including anti-CTLA-4, anti-PD-1, or anti-PD-L1 therapeutic antibody on Protocol GX41563
Exclusion Criteria
Participant actively receiving investigational medicinal product(s) as part of an interventional trial at the time of signing informed consent
This page summarises information from public registry websites, such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc. To learn more about this study, see the For Medical Professional tab or visit one of those websites.
The information is taken directly from public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc., and has not been edited.
Results Disclaimer
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What is Clinical Research?
In clinical research, volunteers, researchers, and medical professionals work together toward a shared goal: better treatment outcomes for patients. Clinical trials are vital to their process. They are carefully designed and follow approved protocols.
For the latest version of this information please go to www.forpatients.roche.com