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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

What this study is about

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.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Receive Ipilimumab Injection
  • 2.Take Nivolumab/Relatlimab
  • 3.Take Sarilumab

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IVInjection / IV

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

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