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