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Study of Sarilumab With Immune Checkpoint Inhibitor Rechallenge in Patients With Clinically Significant Immune Related Adverse Events

Study acronym: IRIS
StatusNot Yet Recruiting
PhasePhase 2
Started2026-10
View on ClinicalTrials.gov ↗
The study will enroll patients with history of malignancy treated with immune checkpoint inhibitors (ICI) that have developed a grade 2 or higher immune related adverse event requiring treatment discontinuation as deemed by the patient's treating physician. Patients will be sequentially enrolled into the single-arm study after meeting the pre-specified eligibility criteria
Trial Details
NCT Number NCT07836101
Lead Sponsor Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Collaborators: Sanofi-Regeneron, Bristol-Myers Squibb
Conditions Any Advanced Solid Tumors
Enrollment 41 participants
Start Date 2026-10
Primary Completion 2029-08 (estimated)
Study Completion 2029-12 (estimated)
Updated on ClinicalTrials.gov 2026-09-23