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Clinical Trial Summary

This single-arm, multicenter clinical study will treat the patient who have relapsed or refractory neuroblastoma with an infusion of the patient's own T cells that have been genetically modified to express a chimeric antigen receptor(CAR)that will bind to tumour cells modified to express the GD2 protein on the cell surface. The study will determine if these modified T cells help the body's immune system eliminate tumour cells .The trial will also study the safety of treatment for CAR-T, how long CAR-T cells stay in the patient's body and the impact on this treatment for survival.


Clinical Trial Description

This is a single-arm, multicenter clinical study to evaluate efficacy and safety of chimeric antigen receptor T cell immunotherapy (CAR-T) in the treatment of relapsed or refractory neuroblastoma in children. The study will be conducted using a phaseⅠ/Ⅱdesign the study will have the following sequential phases: part A (screening, leukapheresis,cell product preparation and cytoreductive chemotherapy) and part B (treatment and follow-up). the follow-up period for each participant is approximately 35 months after the final CAR-T infusion. The total duration of the study are expected to be approximately 3 years. A total of 22 patients may be enrolled over a period of 3 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02919046
Study type Interventional
Source Sinobioway Cell Therapy Co., Ltd.
Contact Yongjun Fang, Ph.D
Phone 18951769586
Email fyj322@189.cn
Status Recruiting
Phase N/A
Start date September 2016
Completion date September 2020

See also
  Status Clinical Trial Phase
Completed NCT02761915 - A Phase I Trial of Anti-GD2 T-cells (1RG-CART) Phase 1