154
Participants
Start Date
November 4, 2022
Primary Completion Date
August 31, 2026
Study Completion Date
May 31, 2027
Prospera
"Prospera™ detects allograft rejection noninvasively and with high accuracy by measuring the fraction of donor derived cell-free DNA (dd-cfDNA) in the patient's blood, without the need for prior donor or recipient genotyping.~Prospera is a commercially available Laboratory Developed Test (LDT) certified under the Clinical Laboratory Improvement Amendments (CLIA). This test has not been cleared or approved by the U.S. Food and Drug Administration (FDA)."
Columbia University Irving Medical Center, New York
Johns Hopkins Hospital, Baltimore
Ohio State University Medical Center, Columbus
Corewell Health, Grand Rapids
Northwestern Memorial Hospital, Chicago
Washington University School of Medicine, St Louis
UT Southwestern Medical Center, Dallas
Baylor College of Medicine Medical Center, Houston
Houston Methodist Hospital, Houston
Cedars-Sinai Medical Center, California City
University of Washington, Seattle
Lead Sponsor
Natera, Inc.
INDUSTRY