Long Term Follow up of Subjects Exposed to Genetically Engineered T Cell Receptors
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|ClinicalTrials.gov Identifier: NCT03391791|
Recruitment Status : Terminated (terminated after participants were enrolled)
First Posted : January 5, 2018
Last Update Posted : January 7, 2021
Subjects who previously took part in an Adaptimmune study and received genetically changed T cells (including but not limited to MAGE-A10ᶜ⁷⁹⁶T and MAGE-A4ᶜ¹º³²T) are asked to take part in this long term follow-up study. Subjects will be asked to join this study once they complete the parent interventional study.
The purpose of this study is to find out if the genetically changed T cells that subjects received in the parent study have any long-term side effects. No additional study drug will be given, but subjects can receive other therapies for their cancer while they are being followed for long term safety in this study.
For a period of 15 years starting from last administration of the genetically changed T cells, subjects will visit their study doctor for a check-up and to have blood tests to look for any changes that might have happened because of the genetically changed T cells.
|Condition or disease||Intervention/treatment|
|Solid and Hematological Malignancies||Genetic: Genetically engineered T Cell Receptors|
This is a non-therapeutic, multi-center, long-term follow-up (LTFU) study of subjects who have received lentivirus-mediated genetically engineered T Cell Receptors in an Adaptimmune sponsored clinical trial. The study is designed in accordance with FDA and EMA guidance on gene therapy trials.
The study involves up to 15 years post-infusion monitoring of subjects who have been exposed to lentivirus-mediated gene transfer in Adaptimmune clinical studies. The study will include subjects who have received various T cell receptors including but not limited to MAGE-A10ᶜ⁷⁹⁶T and MAGE-A4ᶜ¹º³²T. Subjects will undergo clinical evaluation (i.e., new medical history, physical exam, adverse events, and exposure to mutagenic agents, anti-cancer therapies and investigational products in other clinical studies) with careful attention to adverse events possibly related to gene transfer or lentivirus-induced diseases. Blood samples will be collected for evaluating persistence of cells with lentiviral vector sequences, the detection of replication competent lentivirus (RCL), and chemistry and hematology laboratory assessments. Subjects will be followed for survival.
|Study Type :||Observational|
|Actual Enrollment :||2 participants|
|Official Title:||Long Term Follow-up of Subjects Exposed to Genetically Engineered Tumor Antigen Specific T Cell Receptors|
|Actual Study Start Date :||February 28, 2018|
|Actual Primary Completion Date :||July 24, 2018|
|Actual Study Completion Date :||July 24, 2018|
Genetically engineered T Cell Receptor- treated
Long term follow-up of subjects with solid or hematological malignancies who have received lentivirus-mediated genetically engineered T Cell Receptors in a previous trial
Genetic: Genetically engineered T Cell Receptors
No study drug is administered in this study. Subjects who received lentivirus-mediated genetically engineered T Cell Receptors in a previous trial will be evaluated in this trial for long-term safety and efficacy.
- Number of subjects with specific Long Term Follow-Up adverse events (AEs), including serious adverse events (SAEs) associated with administration of autologous T cell receptors that have been genetically modified by lentiviral vectors. [ Time Frame: 15 years post last treatment ]
- New malignancies
- New incidence or exacerbation of a pre-existing neurologic disorder
- New incidence or exacerbation of a prior rheumatologic or other autoimmune disorder
- New incidence of a hematologic disorder
- Opportunistic and/or serious infections
- Unanticipated illness and/or hospitalization deemed related to gene modified cell therapy
- Measurement of Replication Competent Lentivirus (RCL) in genetically modified T cells [ Time Frame: 15 years post last treatment ]Subjects' peripheral blood samples will be used to evaluate RCL
- Persistence of genetically modified cells in the body [ Time Frame: 15 years post last treatment ]Peripheral blood samples will be used to evaluate persistence
- Assess the pattern of vector integration sites if at least 1% of cells in the surrogate sample are positive for vector sequences by PCR [ Time Frame: 15 years post last treatment ]Number of samples positive for vector integration by PCR
- Overall Survival (OS) post-infusion [ Time Frame: 15 years post last treatment ]OS defined as the interval between the date of first T cell infusion and date of death due to any cause
Biospecimen Retention: Samples With DNA
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03391791
|United States, Tennessee|
|Sarah Cannon Research Institute|
|Nashville, Tennessee, United States, 37203|
|United States, Texas|
|University of Texas MD Anderson Cancer Center|
|Houston, Texas, United States, 77030|
|Princess Margaret Cancer Centr|
|Toronto, Ontario, Canada, M5G1X6|
|Principal Investigator:||Marcus Butler, MD||Princess Margaret Cancer Centr|