Long-term Follow-up of Participants Treated With Galapagos Chimeric Antigen Receptor (CAR) T-cell Therapies
Purpose
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.
Condition
- Hematological Malignancies
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
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 Design
- Phase
- Phase 3
- Study Type
- Interventional
- Allocation
- N/A
- Intervention Model
- Single Group Assignment
- Primary Purpose
- Other
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Previously treated participants with GLPG CAR T-cell therapy |
All participants who have been treated with a Galapagos CAR T-cell therapy |
|
Recruiting Locations
Tufts Medical Center
Boston, Massachusetts 02111
Boston, Massachusetts 02111
More Details
- Status
- Recruiting
- Sponsor
- Lakefront Biotherapeutics NV
Study Contact
Lakefront Biotherapeutics Medical Information+3215342900
medicalinfo@lakefrontbio.com