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SEP 2025

PROSTest®: large screening study (800 men) for prostate cancer

MAY 2025

NETest 2.0® submitted to NYSDOH

APR 2025

PROSTest® approved by NYSDOH.

FEB 2025

ISO15189 certification submitted.

JAN 2025

NETest 2.0® developed.

JUN 2024

Finalizing two clinical studies evaluating the PROSTest® as a monitor for 177Lu-PSMA (Pluvicto) radioligand therapy (RLT).

MAY 2024

PROSTest® approved by CLIA and submitted to NYSDOH.

MAR 2024

Completed the evaluation of the PROSTest® as a marker for minimal residual disease (MRD).

MAR 2024

Completed the evaluation of the PROSTest® as a marker for minimal residual disease (MRD).

MAR 2024

Completed the publication of the first article about PROSTest.® (View Paper)

DEC 2023

Completed a screening study on high-risk men of African descent for prostate cancer.

OCT 2023

Completed PROSTest®
clinical validation study.

MAR 2023

Development of the PROSTest® – a molecular genomic assay for prostate cancers.

DEC 2022

CAP certification.

OCT 2020

FDA-EUA for COVID-19 PCR saliva testing.

NOV 2019

Set-up of NETesting at Sarah Cannon, UK.

AUG 2019

FDA-EUA for nasopharyngeal swab SARS-CoV-2 diagnosis.

OCT 2018

Development of the PPQ – PRRT Predictive Quotient.

AUG 2018

New York State Department of Health Permit – NETest.®

MAY 2018

California Department of Health Permit – NETest.®

OCT 2014

Clinical laboratory certification in Connecticut, CLIA license for the NETest.®

JUL 2014

Laboratory establishment, Branford, Connecticut.

The Power of mRNA

While DNA and protein diagnostics are common, we specialize in mRNA. Positioned between DNA and proteins, mRNA in whole blood provides a real-time picture of tumor activity. Our novel preservative ensures stable and reliable testing.

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Pioneering Liquid Biopsy

The initial efforts of Sir Christopher Wren in the 1600’s to conduct research on the intravenous transfer of blood inspired the founders of Wren Laboratories to revolutionize how blood can further provide answers for patient care through revolutionary mRNA liquid biopsy for cancer diagnostics.

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Our Mission at Wren

We deliver innovative machine learning, liquid biopsy-RNA-based in-vitro diagnostics, for the detection of minimal residual disease and prediction of cancer prognosis and response to therapeutics.

2014

Year Wren Laboratories was founded

135

Number of Patents

30

Number of genes analyzed by the PROSTest®

95%

Clinical accuracy for PROSTest® (vs. 48% for PSA)

55

Number of genes analyzed by the NETest®

Precision Oncology Through mRNA Liquid Biopsy

For decades, cancer management relied heavily on imaging, invasive tissue biopsies, and delayed recognition of residual or recurrent disease. Recognizing the need for more sensitive and dynamic molecular monitoring, Wren’s scientific efforts began exploring liquid biopsy technologies in 2004 to detect cancer-associated genetic activity through circulating biomarkers in blood and other non-invasive specimens.

Today, Wren Laboratories focuses on advanced mRNA-based molecular diagnostics and machine learning–enhanced bioinformatics designed to support earlier cancer detection, molecular surveillance, treatment monitoring, and precision oncology applications. By analyzing tumor-associated genetic signatures from blood and saliva, Wren aims to improve detection of minimal residual disease (MRD), recurrence risk assessment, and real-time disease monitoring through minimally invasive testing.

Wren’s growing portfolio includes molecular assays and translational technologies targeting multiple disease areas, including prostate cancer, neuroendocrine tumors, colorectal cancer, pancreatic cancer, lung cancer, melanoma and hematologic malignancies. The company continues to expand its research, clinical collaborations, and technology platforms to advance the future of non-invasive precision diagnostics.

Through a simple blood or saliva sample, Wren is helping transform mRNA liquid biopsy into a practical clinical reality.