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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT05509855
Registration number
NCT05509855
Ethics application status
Date submitted
20/07/2022
Date registered
22/08/2022
Date last updated
5/07/2024
Titles & IDs
Public title
A Long-Term Safety Follow-Up Study for Patients Treat With WU-CART-007
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Scientific title
A Long-Term Safety Follow-Up Study for Patients Treated With Anti-CD7 Allogeneic CAR-T Cells (WU-CART-007)
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Secondary ID [1]
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WUC007-02
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
T-cell Acute Lymphoblastic Leukemia
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T-cell Lymphoblastic Lymphoma
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Condition category
Condition code
Cancer
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Leukaemia - Acute leukaemia
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Cancer
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0
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Lymphoma (non Hodgkin's lymphoma) - High grade lymphoma
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Cancer
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0
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Lymphoma (non Hodgkin's lymphoma) - Low grade lymphoma
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Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Treatment: Other - Genetic: WU-CART-007
Patients treated with WU-CART-007 - Patients who received previous treatment with WU-CART-007
Treatment: Other: Genetic: WU-CART-007
No study drug is administered in this study. Patients who have received WU-CART-007 will be enrolled in this study for Long Term Safety and Efficacy
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Intervention code [1]
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Treatment: Other
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Delayed adverse events (AEs)/serious adverse events (SAEs)
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Assessment method [1]
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assess the risk of delayed adverse events including serious events following exposure to WU-CART-007
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Timepoint [1]
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up to 15 years
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Primary outcome [2]
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Persistence of WU-CART-007 cells
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Assessment method [2]
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Peripheral blood samples will be monitored used polymerase chain reaction for persistence of WU-CART-007 cells
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Timepoint [2]
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Every 6 months for up to 5 years and then yearly for up to 15 years
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Primary outcome [3]
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Tanner Staging
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Assessment method [3]
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Tanner Staging will be used to evaluate growth and development outcomes and sexual maturity status for patients who were \< 18 years of age at the time of treatment with WU CART-007
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Timepoint [3]
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up to 15 years
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Secondary outcome [1]
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Overall survival (OS)
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Assessment method [1]
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To evaluate survival n patients previously treated with WU-CART-007
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Timepoint [1]
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up to 15 years
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Secondary outcome [2]
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Progression-free survival (PFS)
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Assessment method [2]
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To evaluate profession free survival in patients previously treated with WU-CART-007
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Timepoint [2]
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up to 15 years
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Eligibility
Key inclusion criteria
Patients that received WU-CART-007 in the context of any investigational study will be eligible to participate in this long-term follow-up study.
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Minimum age
12
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Not Applicable
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Study design
Purpose
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Duration
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Selection
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
22/08/2022
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
1/07/2037
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Actual
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Sample size
Target
44
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Recruitment hospital [1]
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Peter MacCullam Cancer Center - Melbourne
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Recruitment postcode(s) [1]
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- Melbourne
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Recruitment outside Australia
Country [1]
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United States of America
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State/province [1]
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California
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Country [2]
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United States of America
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State/province [2]
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Missouri
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Country [3]
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United States of America
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State/province [3]
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Pennsylvania
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Wugen, Inc.
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
This study will provide long-term follow-up for patients who have received treatment with WU-CART-007 in a previous clinical trial. In this study, patients will be followed for up to 15 years after their last dose of WU-CART-007 for evaluation of delayed adverse events, presence of persisting WU-CART-007 vector sequences, and overall survival and progression-free survival.
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Trial website
https://clinicaltrials.gov/study/NCT05509855
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Jan Davidson-Moncada, MD, PhD
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Address
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Wugen, Inc.
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT05509855
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