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ACTIVE NOT RECRUITING
NCT05170425

LAMBDA 002 (Lung Registry) Study

Sponsor: Natera, Inc.

View on ClinicalTrials.gov

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

Interventions

DEVICE

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