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RECRUITING
NCT07223411

Opdualag vs. Cemiplimab/Fianlimab in Relation to the Immunological Response in Tumor and Peripheral Blood in Unresectable or Metastatic Melanoma

Sponsor: John Kirkwood

View on ClinicalTrials.gov

Summary

This translational study will examine the immune effector responses of patients who received a two-drug combination for first line therapy by examining tumor and peripheral blood of participants with unresectable locally advanced or metastatic melanoma.

Official title: Dose-response Analysis of Nivolumab/Relatlimab in the Fixed-dosed Combination 'Opdualag' vs. Cemiplimab/Fianlimab in Relation to the Immunological Response in Tumor and Peripheral Blood for Participants With Unresectable or Metastatic Melanoma: A Corollary Study of HCC 24-056 (NCT06246916)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

20

Start Date

2025-11-19

Completion Date

2031-11-01

Last Updated

2025-11-26

Healthy Volunteers

Not specified

Interventions

DRUG

Fianlimab + Cemiplimab

Patients treated with Fianlimab 1600 mg + Cemiplimab 350 mg under protocol NCT06246916

DRUG

Relatlimab + Nivolumab

Patients treated with Relatlimab 160 mg + Nivolumab 480 mg under protocol NCT06246916

Locations (1)

UPMC Hillman Cancer Center

Pittsburgh, Pennsylvania, United States