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Derivation of Primary Donor Cell Lines for Human Cell Reprogramming
This is a research study in which your cells will be used for somatic cell nuclear transfer (SCNT), and/or genetic reprogramming research which may result in the production of stem cell lines. This study does not provide treatment.
It is thought that studies of genetic reprogramming and SCNT using human cells have the potential to give us new basic knowledge about human development. Current work will focus on developing this basic knowledge. In the future, human embryonic stem cell lines (hESC) derived from genetic reprogramming and SCNT may also have the potential to develop into cell types that are useful for cell-based therapies to treat human disease and disability.
Age
1 - 75 years
Sex
ALL
Healthy Volunteers
Yes
Stanford University School of Medicine
Stanford, California, United States
Start Date
September 1, 2007
Primary Completion Date
January 1, 2030
Completion Date
January 1, 2030
Last Updated
August 12, 2022
60
ESTIMATED participants
Improving the scientific process of human cell reprogramming
PROCEDURE
Lead Sponsor
Stanford University
NCT06826365
NCT07153367
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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