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Study to Create Potential Cell-Based Therapies to Treat Human Disease and Disability

Infertility Clinical Trial

Official title:
Derivation of Primary Donor Cell Lines for Human Cell Reprogramming

Clinical Trial Summary

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.

Clinical Trial Description

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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00628199
Study type Observational
Source Stanford University
Contact
Status Enrolling by invitation
Phase
Start date September 2007
Completion date January 2030
View Details
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