Viewing Study NCT05002569


Ignite Creation Date: 2025-12-24 @ 10:46 PM
Ignite Modification Date: 2026-01-01 @ 12:54 PM
Study NCT ID: NCT05002569
Status: TERMINATED
Last Update Posted: 2025-05-18
First Post: 2021-08-04
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: A Study to Assess Adjuvant Immunotherapy With Nivolumab Plus Relatlimab Versus Nivolumab Alone After Complete Resection of Stage III-IV Melanoma
Sponsor: Bristol-Myers Squibb
Organization:

Study Overview

Official Title: A Phase 3, Randomized, Double-blind Study of Adjuvant Immunotherapy With Nivolumab + Relatlimab Fixed-dose Combination Versus Nivolumab Monotherapy After Complete Resection of Stage III-IV Melanoma
Status: TERMINATED
Status Verified Date: 2025-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Inability to meet protocol objectives
Has Expanded Access: True
If Expanded Access, NCT#: NCT05170685
Has Expanded Access, NCT# Status: NO_LONGER_AVAILABLE
Acronym: RELATIVITY-098
Brief Summary: The purpose of this study is to assess nivolumab plus relatlimab fixed-dose combination (FDC) versus nivolumab alone in participants with completely resected stage III-IV melanoma.
Detailed Description: None

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
2021-001641-13 EUDRACT_NUMBER None View