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ACTIVE NOT RECRUITING
NCT06561425
PHASE1/PHASE2

A Study Evaluating the Safety and Efficacy of GLPG5101 (19CP02) in Participants With Non-Hodgkin Lymphoma

Sponsor: Galapagos NV

View on ClinicalTrials.gov

Summary

This study is evaluating whether an experimental treatment called GLPG5101 helps to treat non-Hodgkin lymphoma (NHL) and if it is safe to use. This study will be carried out in 2 phases: * The first phase is to see which doses of GLPG5101 work best with the least number of side effects. * In the second phase, participants will receive the selected dose(s) based on the results in the first phase.

Official title: A Phase I/II, Multicenter Study Evaluating the Feasibility, Safety, and Efficacy of Point-of-care Manufactured GLPG5101 (19CP02) in Subjects With Relapsed/Refractory B-cell Non-Hodgkin Lymphoma

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

130

Start Date

2022-03-09

Completion Date

2029-07-01

Last Updated

2026-03-16

Healthy Volunteers

No

Interventions

GENETIC

GLPG5101

Autologous anti-CD19 chimeric antigen receptor (CAR) T cell therapy

Locations (10)

Tufts Medical Center

Boston, Massachusetts, United States

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States

Dana-Farber Cancer Institute

Boston, Massachusetts, United States

Antwerp University Hospital

Edegem, Belgium

UZ Leuven

Leuven, Belgium

CHU De Liège

Liège, Belgium

Cliniques Universitaires Saint-Luc

Woluwe-Saint-Lambert, Belgium

Academisch Medisch Centrum

Amsterdam, Netherlands

Leiden University Medical Center

Leiden, Netherlands

Erasmus Universitair Medisch Centrum Rotterdam (Erasmus MC)

Rotterdam, Netherlands