APOL1 Long-term Kidney Transplantation Outcomes Network (APOLLO)

The APOLLO study is being done in an attempt to improve outcomes after kidney transplantation and to improve the safety of living kidney donation based upon variation in the apolipoprotein L1 gene (APOL1). Genes control what is inherited from a family, such as eye color or blood type. Variation in APOL1 can cause kidney disease. African Americans, Afro-Caribbeans, Hispanic Blacks, and Africans are more likely to have the APOL1 gene variants that cause kidney disease. APOLLO will test DNA from kidney donors and recipients of kidney transplants for APOL1 to determine effects on kidney transplant-related outcomes.

CT.gov Identifier
EudraCT Identifier
N/A
CTIS:
N/A
Sponsor
National Institutes of Health/National Institute of Allergy and Infectious Diseases
Collaborator
Wake Forest University Health Sciences, National Institute of Health & Family Welfare (NIHFW)
Study Contact Information
N/A
Recruiting
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Study Details

Diseases
APOL1 Mediated Kidney Disease (AMKD)
Study Drug
No drug
Genes
APOL1
Study Dates
Mar 2019 - May 2027
Sex
Female & Male
Age
N/A

Protocol Summary

The APOLLO study is being done in an attempt to improve outcomes after kidney transplantation and to improve the safety of living kidney donation based upon variation in the apolipoprotein L1 gene (APOL1). Genes control what is inherited from a family, such as eye color or blood type. Variation in APOL1 can cause kidney disease. African Americans, Afro-Caribbeans, Hispanic Blacks, and Africans are more likely to have the APOL1 gene variants that cause kidney disease. APOLLO will test DNA from kidney donors and recipients of kidney transplants for APOL1 to determine effects on kidney transplant-related outcomes.

Study Locations

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