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Study details
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Sarilumab Trial for Melanoma

NYU Langone Health
NCT IDNCT05428007ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

105

Study length

about 5.1 years

Ages

18–100

Locations

4 sites in CA, MA, NY

About this study

This trial is testing a new treatment called sarilumab, when combined with ipilimumab, nivolumab and relatlimab, in people with unresectable melanoma. The goal is to see if this combination can be safe, well-tolerated, and effective at treating the cancer.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Receive Ipilimumab Injection
  • 2.Take Nivolumab/Relatlimab
  • 3.Take Sarilumab
PhasePhase 2
DrugIpilimumab Injection
Routeinjection
Primary goalNumber of Grades 3-5 Treatment-Related Immune-Related Adverse Events (irAE) per NCI CTCAE v 5.0 Criteria

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low8%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

ipilimumab (Immune checkpoint inhibitor; blocks CTLA-4 on T cells), nivolumab (Immune checkpoint inhibitor; blocks PD-1 receptor on T cells), Antineoplastic Agent [TC] (Antibody-Receptor Interactions), sarilumab

Drug routes

injection (Injection), infusion

Endpoints

Primary: Number of Grades 3-5 Treatment-Related Immune-Related Adverse Events (irAE) per NCI CTCAE v 5.0 Criteria

Secondary: Best overall response (iBOR), Disease Control Rate (DCR), Duration of Immune-related Overall Response, Duration of Overall Response, Immune-related Disease Control Rate per irRC criteria, Immune-related Progression-Free Survival (irPFS), Immune-related Response Rate (irRR) per irRC criteria, Overall survival (OS)

Body systems

Oncology