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TERMINATED
NCT06561425
PHASE1/PHASE2

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

Sponsor: Lakefront Biotherapeutics 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

2026-05-27

Last Updated

2026-06-30

Healthy Volunteers

No

Interventions

GENETIC

GLPG5101

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

Locations (11)

Tufts Medical Center

Boston, Massachusetts, United States

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States

Antwerp University Hospital

Edegem, Belgium

UZ Leuven

Leuven, Belgium

CHU De Liège

Liège, Belgium

Algemeen Ziekenhuis Delta

Roeselare, Belgium

Cliniques Universitaires Saint-Luc

Woluwe-Saint-Lambert, Belgium

Helsingin Yliopistollinen Sairaala (HUS)

Helsinki, Finland

Academisch Medisch Centrum (Amsterdam UMC)

Amsterdam, Netherlands

Leiden University Medical Center

Leiden, Netherlands

Erasmus Universitair Medisch Centrum Rotterdam (Erasmus MC)

Rotterdam, Netherlands