Experiences w/ & Attitudes Towards Immune Chckpt Inhibitors in NSCLC Patients Single Center Survey Based Study
Part of paid clinical trials in Los Angeles, California.
- Sponsor
- University of Southern California
- Study ID
- NCT07339254
- Status
- Recruiting
Conditions
- Lung Non-Small Cell Carcinoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Non-Interventional Study — OTHERNon-interventional study
Study Details
This study evaluates patient satisfaction with receiving intravenous (IV) and/or subcutaneous (SC) immunotherapy and to assess patient preference for IV immunotherapy administration versus SC immunotherapy administration either at the hospital or at home.
Key Dates
- Start date
- Mar 12, 2026
- Status verified
- Mar 2026
- Primary completion
- Mar 12, 2027
- Completion
- Mar 12, 2028
Study Design
- Enrollment
- 40 participants (estimated)
Arms
- Arm: ObservationalPatients complete surveys on study.
Primary Outcome Measure
Strength of patient perception of Intravenous (IV) Immune Checkpoint Inhibitor (ICI) therapy [ Time Frame: At Baseline through study completion, up to 1 year. ]
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Los Angeles General Medical Center | Los Angeles | California | 90033 | Robert Hsu (PRINCIPAL_INVESTIGATOR) |
| USC / Norris Comprehensive Cancer Center | Los Angeles | California | 90033 | Robert Hsu (PRINCIPAL_INVESTIGATOR) |
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