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LAMBDA 002 (Lung Registry) Study
Sponsor: Natera, Inc.
Summary
The LAMBDA 002 registry study is an observational, longitudinal, multi-center study observing patients undergoing lung transplant.
Official title: Observational Registry Study With Sub-analysis (Patients Previously Randomized to LAMBDA 001) to Assess ProsperaTM Performance for Detection of CLAD After Lung Transplant (LAMBDA 002)
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
154
Start Date
2022-11-04
Completion Date
2027-05
Last Updated
2025-05-22
Healthy Volunteers
No
Conditions
Interventions
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).
Locations (11)
Cedars-Sinai Medical Center
California City, California, United States
Northwestern Memorial Hospital
Chicago, Illinois, United States
Johns Hopkins Hospital
Baltimore, Maryland, United States
Corewell Health
Grand Rapids, Michigan, United States
Washington University School of Medicine
St Louis, Missouri, United States
Columbia University Irving Medical Center
New York, New York, United States
Ohio State University Medical Center
Columbus, Ohio, United States
UT Southwestern Medical Center
Dallas, Texas, United States
Baylor College of Medicine Medical Center
Houston, Texas, United States
Houston Methodist Hospital
Houston, Texas, United States
University of Washington
Seattle, Washington, United States