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Clinical Trial Summary

Collect DNA from well-characterized healthy volunteers.


Clinical Trial Description

DNA and plasma will be used to identify and determine allele frequencies of genetic variants in membrane transporters and other genes relevant to human disease or drug response, including drug metabolizing enzymes, collagen, race/ethnicity, neurovascular disease, asthma/allergy/lung disease, and cardiovascular disease. This phase of the study will serve as the hypothesis-generating phase for future studies by identifying genetic variants and determining allele frequencies among an ethnically diverse cohort of healthy volunteers. Future investigations (separate IRB applications) will attempt to correlate genotypes to phenotypes among this cohort of volunteers. The allele identification and frequency data from this group of healthy volunteers will also be used to design association studies in relevant disease populations. Determine if identified sequence variants are associated with gain or loss of in vitro biologic function using lymphocytes obtained from patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00187668
Study type Observational
Source University of California, San Francisco
Contact
Status Completed
Phase
Start date February 2004
Completion date August 2023

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