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 the NCT# and Site #.


BMS Clinical Trials Contact Center www.BMSClinicalTrials.com 8559073286
Clinical.Trials@bms.com


Study Location:

Skip to Main Content
English | Cymraeg
Be Part of Research - Trial Details - A Study to Compare the Efficacy and Safety of Golcadomide in Combination With Rituximab (Golca + R) vs Investigator's Choice in Participants With Relapsed/Refractory Follicular Lymphoma Who Have Received at Least 1 Prior Line of Systemic Therapy (GOLSEEK-4)

A Study to Compare the Efficacy and Safety of Golcadomide in Combination With Rituximab (Golca + R) vs Investigator's Choice in Participants With Relapsed/Refractory Follicular Lymphoma Who Have Received at Least 1 Prior Line of Systemic Therapy (GOLSEEK-4)

Recruiting

Open to: ALL

Age: 18.0 - N/A

Medical Conditions

Follicular Lymphoma


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 study is designed as a multicenter, randomized, open label Phase 3 study to compare the efficacy and safety of golcadomide in combination with rituximab vs investigator's choice in participants with relapsed/refractory follicular lymphoma who have received at least one line of prior systemic therapy.

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:

Jul 2025 Apr 2028

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : Specified dose on specified days

Intervention Arm Group : Golcadomide + Rituximab;

Intervention Type : DRUG
Intervention Description : Specified dose on specified days

Intervention Arm Group : Golcadomide + Rituximab;Rituximab + Lenalidomide/Chemotherapy;

Intervention Type : DRUG
Intervention Description : Specified dose on specified days

Intervention Arm Group : Rituximab + Lenalidomide/Chemotherapy;

Intervention Type : DRUG
Intervention Description : Specified dose on specified days

Intervention Arm Group : Rituximab + Lenalidomide/Chemotherapy;

Intervention Type : DRUG
Intervention Description : Specified dose on specified days

Intervention Arm Group : Rituximab + Lenalidomide/Chemotherapy;

Intervention Type : DRUG
Intervention Description : Specified dose on specified days

Intervention Arm Group : Rituximab + Lenalidomide/Chemotherapy;

Intervention Type : DRUG
Intervention Description : Specified dose on specified days

Intervention Arm Group : Rituximab + Lenalidomide/Chemotherapy;

Intervention Type : DRUG
Intervention Description : Specified dose on specified days

Intervention Arm Group : Rituximab + Lenalidomide/Chemotherapy;



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.

  • Norfolk and Norwich University Hospitals NHS Foundation Trust
    Cringleford
    England
    NR4 7UY
  • Kent and Canterbury Hospital
    Canterbury
    Kent
    CT1 3NG
  • The Christie NHS Foundation Trust
    Manchester
    M20 4BX

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


BMS Clinical Trials Contact Center www.BMSClinicalTrials.com 8559073286
Clinical.Trials@bms.com



The study is sponsored by Celgene




We'd like your feedback

Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.


Is this study information helpful?

What will you do next?

Read full details for Trial ID: NCT06911502
Last updated 18 May 2026

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.