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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 development of allogeneic cellular immunotherapy products.


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 (except for the basic biological indicators of UCAR-T product preparation) will receive peripheral venous whole blood sampling, and the volunteers receiving apheresis based on the assessment results will be enrolled. 2. Apheresis period: 5 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

  • Collection of Peripheral Blood Mononuclear Cells by Means of Apheresis

NCT number NCT04027855
Study type Interventional
Source The First Affiliated Hospital with Nanjing Medical University
Contact
Status Terminated
Phase N/A
Start date September 26, 2019
Completion date December 9, 2021