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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04833504
Other study ID # I20200011057
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 1, 2018
Est. completion date October 1, 2020

Study information

Verified date January 2021
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This study is designed to monitor all patients exposed to CD19 CAR-T expressing IL7 and CCL19 for 5 years following infusion, to assess their long-term efficacy, including the CAR-vector persistence, the normal immunity rebuilding and the risk of delayed adverse events (AEs).


Description:

Patients are enrolled following completion from the early clinical study of CD19-7X19 CAR-T treatment ( NCT03258047) and will be followed for 5 years post treatment from the last treatment. They will be monitored for safety and efficacy with the primary treatment protocols for the protocol defined duration. This long-term following up study allow an interim analysis to evaluate the outcomes of the study when it arrives in 2 years Collection of such long term effects of CAR-T cell therapy will help to further define the risk-benefit profile of CAR-T Therapies.


Recruitment information / eligibility

Status Completed
Enrollment 39
Est. completion date October 1, 2020
Est. primary completion date October 1, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - All patients who have received the CD19-IL7/CCL19 CAR-T therapy in the earlier enrolled clinical trail and met including and excluding criteria criteria (NCT0325847) Patients who have provided informed consent for the long term follow up study prior to their study participation . Exclusion Criteria: - There are no specific exclusion criteria for this study.

Study Design


Intervention

Biological:
CD19 CAR-T Expressing IL7 and CCL19
A fourth generation CD19 targeting CAR-T expressing IL7 and CCL19

Locations

Country Name City State
China Hui Liu Hangzhou State...

Sponsors (1)

Lead Sponsor Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluate the efficacy of CD19-IL7/CCL19 CAR-T Evaluate the efficacy of CD19-IL7/CCL19 CAR-T including duration of response, progression-free survival, overall surviva and objective response rate (CR + PR) . 5 years
Secondary Evaluate the persistence of CAR-T cells Levels and persistence of CAR+ T cells in serum samples 5 years
Secondary Evaluate the incidence of adverse events The incidence of CRS and CRES; Levels and persistence of cytokines in serum samples;Proportion of patients who relapse or progress among patients who had not relapsed or progressed at study entry/re-entry;Incidence of death ;B- and T- lymphocyte count; 5 years
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