This is a long-term follow-up study for participants treated with Galapagos (GLPG) CAR T-cell therapies to evaluate the long-term safety and efficacy of GLPG CAR T-cell products for 15 years post infusion. Per Health Authorities guidelines for gene therapy medicinal products that utilize integrating vectors (e.g. lentiviral vectors), long term safety and efficacy follow up of treated patients is required. The purpose of this study is to monitor all participants exposed to GLPG CAR T-cell therapies for 15 years following their last CAR T-cell infusion to assess the risk of delayed adverse events (AEs) and the long-term benefit/risk profile and to monitor for replication-competent lentivirus (RCL) and CAR-T cell persistence.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
546
No investigational products will be administered to participants in this study.
Tufts Medical Center
Boston, Massachusetts, United States
RECRUITINGAntwerp University Hospital
Edegem, Belgium
RECRUITINGUniversitair Ziekenhuis Leuven
Leuven, Belgium
RECRUITINGCentre Hospitalier Universitaire (CHU) De Liège
Liège, Belgium
RECRUITINGAlgemeen Ziekenhuis Delta
Roeselare, Belgium
RECRUITINGCliniques Universitaires Saint-Luc
Woluwe-Saint-Lambert, Belgium
RECRUITINGhelsingin yliopistollinen sairaala comprehensive cancer center (HUS)
Helsinki, Finland
RECRUITINGAcademisch Medisch Centrum (Amsterdam UMC)
Amsterdam, Netherlands
RECRUITINGLeids University Medical Center (LUMC)
Leiden, Netherlands
RECRUITINGErasmus Medisch Centrum
Rotterdam, Netherlands
RECRUITING...and 1 more locations
Percentage of participants with targeted adverse events (AEs)
Time frame: From infusion up to 15 years
Percentage of participants with detectable CAR transgene levels in peripheral blood
Time frame: From infusion up to 15 years
Percentage of participants with serious AEs (SAEs) considered related to the Galapagos CAR T-cell therapy
Time frame: From infusion up to 15 years
Percentage of participants with at least 1% of T-cells in the blood sample or positive new malignancies
Time frame: From infusion up to 15 years
Percentage of participants with detectable replication-competent lentivirus (RCL) in peripheral blood
Time frame: From infusion up to 15 years
Percentage of participants who died with causes
Time frame: From infusion up to 15 years
Percentage of participants with disease progression
Time frame: From infusion up to 15 years
Time to subsequent anticancer therapy
Time frame: From infusion up to 15 years
Overall survival
Time frame: From infusion up to 15 years
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