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Clinical Trial Summary

The objective of the study is to collect peripheral blood mononuclear cells (PBMC) from healthy volunteers for the research and production of UCAR T cells used for Clinical trails.


Clinical Trial Description

The study is a single-center study. 1. Screening period: All volunteers are required to sign a written informed consent form for the study; after the signing of informed consent form, the demographic data and medical history of the volunteers will be collected, and physical examinations and local laboratory tests will be performed to assess the eligibility of the volunteers. Volunteers who meet all the inclusion criteria and do not meet any exclusion criteria will receive peripheral venous whole blood sampling, and the volunteers receiving apheresis based on the assessment results will be enrolled. 2. Apheresis period: 25 volunteers who meet the inclusion criteria will undergo collection of peripheral blood mononuclear cells (PBMC) by means of apheresis. ;


Study Design


Related Conditions & MeSH terms

  • Peripheral Blood Mononuclear Cell

NCT number NCT04963959
Study type Interventional
Source The First Affiliated Hospital of Soochow University
Contact chengcheng Fu
Phone +86 13962191404
Email fuchengchengsz@163.com
Status Recruiting
Phase N/A
Start date July 14, 2021
Completion date January 31, 2022

See also
  Status Clinical Trial Phase
Recruiting NCT04448509 - Peripheral Blood Mononuclear Cell Collection Protocol for UCART Cell Tumor Immunotherapy Study N/A
Completed NCT02272530 - Analysis of Proteome and Pathophysiological Characteristics of Human Blood Cells