LAMBDA 002 (Lung Registry) Study

Active, not recruitingOBSERVATIONAL
Enrollment

154

Participants

Timeline

Start Date

November 4, 2022

Primary Completion Date

August 31, 2026

Study Completion Date

May 31, 2027

Conditions
Lung Transplant Rejection
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)."

Trial Locations (11)

10032

Columbia University Irving Medical Center, New York

21287

Johns Hopkins Hospital, Baltimore

43210

Ohio State University Medical Center, Columbus

49503

Corewell Health, Grand Rapids

60611

Northwestern Memorial Hospital, Chicago

63110

Washington University School of Medicine, St Louis

75390

UT Southwestern Medical Center, Dallas

77030

Baylor College of Medicine Medical Center, Houston

Houston Methodist Hospital, Houston

90048

Cedars-Sinai Medical Center, California City

98195

University of Washington, Seattle

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Natera, Inc.

INDUSTRY

NCT05170425 - LAMBDA 002 (Lung Registry) Study | Biotech Hunter | Biotech Hunter