APOL1 Long-term Kidney Transplantation Outcomes Network (APOLLO)
Launched by WAKE FOREST UNIVERSITY HEALTH SCIENCES · Jul 30, 2018
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
The APOLLO study is a clinical trial aimed at improving the outcomes of kidney transplants and ensuring the safety of living kidney donations. It focuses on a specific gene called apolipoprotein L1 (APOL1), which can affect kidney health. This gene is more common among individuals of African ancestry, and certain variations can increase the risk of kidney disease. By testing the DNA of both kidney donors and recipients for APOL1 variations, researchers hope to understand how these genetic factors might influence the success of kidney transplants.
To participate in this study, living kidney donors must have African ancestry, which includes groups such as African Americans, Afro-Caribbeans, Hispanic Blacks, or Africans. It's important for potential donors to be willing to provide informed consent to participate. While enrollment for kidney transplant recipients has ended, the trial will continue to recruit living donors for the next two years. Participants can expect to contribute a DNA sample and be part of a study that may help improve kidney transplant outcomes for future patients.
Gender
ALL
Eligibility criteria
- Inclusion Criteria for Living Donors:
- • Living kidney donors with self-reported recent African ancestry (defined as African American, Afro-Caribbean, Hispanic black or African) will be eligible for inclusion.
- Exclusion Criteria for Living Donors:
- • Participants who are unable or unwilling to provide informed consent.
- • Enrollment and bio sample collection from deceased donors at OPOs ended on May 31, 2023 and recruiting kidney transplant recipients ended on June 15, 2023.
- • Phase II started on 9/1/2023 and only Living Donors will be recruited for an additional 2 years.
About Wake Forest University Health Sciences
Wake Forest University Health Sciences is a leading academic research institution dedicated to advancing healthcare through innovative clinical trials and translational research. With a strong emphasis on multidisciplinary collaboration, the organization leverages its extensive expertise in medical research, patient care, and education to develop and evaluate new therapies and interventions. Committed to improving patient outcomes and public health, Wake Forest University Health Sciences fosters a dynamic environment for scientific inquiry, engaging in a wide range of clinical studies that address pressing health challenges. Through its rigorous methodologies and ethical standards, the institution aims to contribute significantly to the medical field and enhance the quality of life for diverse populations.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Philadelphia, Pennsylvania, United States
Baltimore, Maryland, United States
Birmingham, Alabama, United States
Baltimore, Maryland, United States
Cleveland, Ohio, United States
Nashville, Tennessee, United States
Durham, North Carolina, United States
San Francisco, California, United States
Baltimore, Maryland, United States
Winston Salem, North Carolina, United States
Madison, Wisconsin, United States
New York, New York, United States
New York, New York, United States
Atlanta, Georgia, United States
New York, New York, United States
Miami, Florida, United States
Boston, Massachusetts, United States
Ann Arbor, Michigan, United States
Saint Louis, Missouri, United States
Patients applied
Trial Officials
Barry I. Freedman, MD
Principal Investigator
Wake Forest University Health Sciences
David M. Reboussin, PhD
Principal Investigator
Wake Forest University Health Sciences
Paul L. Kimmel, MD
Study Director
Natl Institute of Diabetes, Digestive & Kidney Diseases
Marva Moxey-Mims, MD
Study Chair
Children's Natl Health System; George Washington Univ Sch of Med and Health Serv
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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