This study evaluates the symptoms that immune checkpoint inhibitors may cause in patients with cutaneous melanoma.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT07148245.
Locations matching your search criteria
United States
California
San Francisco
University of California San FranciscoStatus: Active
Contact: Carolyn S. Harris
Phone: 415-353-7668
PRIMARY OBJECTIVES:
I. Evaluate for changes over time in the symptom experience of patients with stage IIB to IV cutaneous melanoma receiving an immune checkpoint inhibitor.
II. Identify distinct symptom profiles over time.
III. Evaluate for demographic, clinical, environmental, and molecular risk factors associated with a worse symptom profile over time.
OUTLINE: This is an observational study.
Patients complete questionnaires and undergo blood sample collection at time of standard of care blood collection on study.
Trial PhaseNo phase specified
Trial TypeNot provided by clinicaltrials.gov
Lead OrganizationUniversity of California San Francisco
Principal InvestigatorCarolyn S. Harris