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Compound · clinical trials

Relatlimab

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 11 trials in our USA, UK, Ireland, India and China registers that name Relatlimab as an intervention. Synced 24 Sep 2026
11Trials tracked
7Recruiting now
6Lead sponsors
5Country registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards

Relatlimab is named as a drug or biological intervention in 11 clinical trials in our USA, UK, Ireland, India and China trial registers, 7 of which are recruiting. Lead sponsors include Bristol-Myers Squibb (6), Immunocore Ltd (1) and Exelixis (1). Registered phases: Phase 3, Phase 2, Phase 2/3, Phase 1 and Phase 4. Conditions studied include Melanoma; Advanced Melanoma; Non-small Cell Lung Cancer.

01

Clinical trials of Relatlimab

11 trials
NCT IDStudyPhaseStatusLead sponsorRegister
NCT06112314 IMC-F106C Regimen Versus Nivolumab Regimens in Previously Untreated Advanced Melanoma (PRISM-MEL-301) (ClinicalTrials.gov ↗)
Advanced Melanoma
Phase 3 Recruiting Immunocore Ltd UK, USA
NCT06246916 A Study With Combinations of Anti-LAG-3 and Anti-PD-1 Antibodies in Adult Participants With Advanced or Metastatic Melanoma (Harmony Head-to-Head) (ClinicalTrials.gov ↗)
Melanoma
Phase 3 Recruiting Regeneron Pharmaceuticals USA
NCT06264180 VO and Nivolumab vs Physician's Choice in Advanced Melanoma That Progressed on Anti-PD-1 & Anti-CTLA-4 Drugs [IGNYTE-3] (ClinicalTrials.gov ↗)
Advanced Melanoma
Phase 3 Recruiting Replimune, Inc. UK, USA
NCT06561386 A Study to Compare the Efficacy of Nivolumab and Relatlimab Plus Chemotherapy vs Pembrolizumab Plus Chemotherapy for Stage IV/Recurrent Non-squamous Non-small Cell Lung Cancer With PD-L1 Expression โ‰ฅ 1%
Non-small Cell Lung Cancer
Phase 3 Recruiting Bristol-Myers Squibb Ireland, UK, USA, India, China
NCT06743126 SUPRAME-ACTengineยฎ IMA203 vs. Investigator's Choice of Treatment in Previously Treated, Unresectable or Metastatic Cutaneous Melanoma (ClinicalTrials.gov ↗)
Melanoma, Cutaneous Malignant
Phase 3 Recruiting Immatics US, Inc. UK, USA
NCT03899155 Pan Tumor Rollover Study
Cancer
Phase 2 Recruiting Bristol-Myers Squibb Ireland, UK, USA, China
NCT05176483 Study of Zanzalintinib in Combination With Immuno-Oncology or Other Agents in Participants With Solid Tumors (ClinicalTrials.gov ↗)
Renal Cell Carcinoma (RCC), Metastatic Castration-Resistant Prostate Cancer (mCRPC), Urothelial Carcinoma (UC)
Phase 1 Recruiting Exelixis UK, USA
NCT07459543 A Study to Assess the Safety, and Tolerability of Nivolumab + Relatlimab Fixed-Dose Combination (FDC) In Unresectable or Metastatic Melanoma Participants In India (ClinicalTrials.gov ↗)
Unresectable Melanoma, Metastatic Melanoma
Phase 4 Not yet open Bristol-Myers Squibb India
NCT05625399 A Study of Subcutaneous Nivolumab + Relatlimab Fixed-dose Combination (FDC) in Previously Untreated Metastatic or Unresectable Melanoma (ClinicalTrials.gov ↗)
Melanoma
Phase 3 Active, closed Bristol-Myers Squibb UK, USA
NCT03470922 A Study of Relatlimab Plus Nivolumab Versus Nivolumab Alone in Participants With Advanced Melanoma (ClinicalTrials.gov ↗)
Melanoma
Phase 2/3 Active, closed Bristol-Myers Squibb UK, USA
NCT06101134 A Study to Evaluate Whether Participants With Melanoma Prefer Subcutaneous vs Intravenous Administration of Nivolumab and Nivolumab + Relatlimab Fixed-dose Combinations (ClinicalTrials.gov ↗)
Melanoma
Phase 2 Active, closed Bristol-Myers Squibb USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied

11 conditions
Condition (as registered)Trials
Melanoma4
Advanced Melanoma2
Non-small Cell Lung Cancer1
Cancer1
Renal Cell Carcinoma (RCC)1
Metastatic Castration-Resistant Prostate Cancer (mCRPC)1
Urothelial Carcinoma (UC)1
Solid Tumor1
Melanoma, Cutaneous Malignant1
Unresectable Melanoma1
Metastatic Melanoma1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Bristol-Myers Squibb6
Immunocore Ltd1
Exelixis1
Replimune, Inc.1
Immatics US, Inc.1
Regeneron Pharmaceuticals1
04

Trials by country register

A trial with sites in more than one country appears in each of those registers.

How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records โ€” it is not written from memory, and nothing here describes how Relatlimab works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Relatlimab (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 24 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician โ€” our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us โ€” we correct promptly and log it.