Ask to take part

Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

First line of the email MUST contain NCT # and Site #.


BMS Study Connect Contact Center www.BMSStudyConnect.com 855-907-3286
Clinical.Trials@bms.com


Study Location:

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Be Part of Research - Trial Details - A Study to Evaluate the Safety, Tolerability, Drug Levels, and Preliminary Efficacy of Relatlimab Plus Nivolumab in Pediatric and Young Adults With Hodgkin and Non-Hodgkin Lymphoma

A Study to Evaluate the Safety, Tolerability, Drug Levels, and Preliminary Efficacy of Relatlimab Plus Nivolumab in Pediatric and Young Adults With Hodgkin and Non-Hodgkin Lymphoma

Recruiting

Open to: ALL

Age: N/A - 30.0

Medical Conditions

Lymphoma
Lymphoma, Non-Hodgkin
Hodgkin Disease


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


The purpose of this study is to assess the safety, tolerability, drug levels, and preliminary efficacy of relatlimab plus nivolumab in pediatric and young adult participants with recurrent or refractory classical Hodgkin lymphoma and non-Hodgkin lymphoma.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Sep 2022 Jul 2028

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : Specified Dose on Specified Days

Intervention Arm Group : Relatlimab + Nivolumab;

Intervention Type : DRUG
Intervention Description : Specified Dose on Specified Days

Intervention Arm Group : Relatlimab + Nivolumab;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Cambridge University Hospitals NHS Foundation Trust
    Cambridge
    Cambridgeshire
    CB2 0QQ
  • Local Institution - 0003
    Nottingham
    Nottinghamshire
    NG5 1PB
  • Local Institution - 0050
    Bristol
    Somerset
    BS2 8BJ
  • Local Institution - 0031
    Birmingham
    West Midlands
    B4 6NH
  • Local Institution - 0068
    Newcastle upon Tyne
    NE1 4LP
  • UCLH
    London
    Londonderry
    NW1 2PG
  • Alder Hey Children's NHS Foundation Trust
    Liverpool
    England
    L12 2AP
  • The Royal Marsden NHS Foundation Trust - Royal Marsden Hospital (RMH) - Sutton
    London
    SM2 5PT

First line of the email MUST contain NCT # and Site #.


BMS Study Connect Contact Center www.BMSStudyConnect.com 855-907-3286
Clinical.Trials@bms.com



The study is sponsored by Bristol-Myers Squibb




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Read full details for Trial ID: NCT05255601
Last updated 27 March 2025

This page is to help you find out about a research study and if you may be able to take part

You can print or share the study information with your GP/healthcare provider or contact the research team directly.