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Long-term Follow-up of Participants Treated with Galapagos Chimeric Antigen Receptor (CAR) T-cell Therapies (Hesperia)

A long-term follow-up study for patients treated with Galapagos CAR T-cell therapies.

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Hematologic malignancies
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All genders
person-wave 18+
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Overview

Principal Investigator: Andreas Klein, MD

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.

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Latoya Marshall

Study details

Inclusion Criteria
  • All participants who have been treated with a Galapagos CAR T-cell therapy in a clinical trial or Managed Access Program.
Exclusion Criteria
  • There are no exclusion criteria for this study
Study Requirements

Experimental: Previously treated participants with GLPG CAR T-cell therapy
- All participants who have been treated with a Galapagos CAR T-cell therapy

Genetic: GLPG CAR T-cell therapy
- No investigational products will be administered to participants in this study.

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