Verici Dx — Immunodiagnostics for kidney transplants

Verici Dx — Immunodiagnostics for kidney transplants

Verici Dx is an immunodiagnostics company focused on the development of tests for the kidney transplantation market. These tests use next-generation RNA sequencing to create a defined risk profile for transplant patients, allowing the tailoring of immunosuppressive therapy and identification of rejection events. The company has two lead products, the pre-transplant test Clarava, and a post-transplant early prognostic called Tuteva, both of which are in clinical validation trials. A third product, Protega, is under development for the prediction of fibrosis and long-term graft failure. Data for these trials are expected to be reported in Q122, with plans in place to commercialise both products quickly afterwards.

Harry Shrives

Written by

Harry Shrives

Associate Analyst

Verici Dx

Immunodiagnostics for kidney transplants

Healthcare

QuickView

20 January 2022

Price

49p

Market cap

£69m

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Share details

Code

VRCI

Listing

AIM

Shares in issue

141m

Business description

Verici Dx is a biotechnology company focused on the development of immuno-diagnostic tests for kidney transplantation. Two tests are in clinical validation trials: Clarava, for pre-transplantation immune profiling, and Tuteva, which tests for rejection events post-transplant.

Bull

Clear market opportunity supported by demand from both clinicians and researchers.

Very little, if any, competition for Clarava and Tuteva.

Plans for commercialisation in 2022 well underway, pending clinical validation.

Bear

Company is subject to research and development risk.

The COVID-19 pandemic may affect clinical validation timelines.

If commercialisation is slower than expected, the company could require further funding before reaching break-even/profitability.

Analyst

Harry Shrives

+44 (0)20 3077 5700

Jacob Thrane

+44 (0)20 3077 5700

Verici Dx is an immunodiagnostics company focused on the development of tests for the kidney transplantation market. These tests use next-generation RNA sequencing to create a defined risk profile for transplant patients, allowing the tailoring of immunosuppressive therapy and identification of rejection events. The company has two lead products, the pre-transplant test Clarava, and a post-transplant early prognostic called Tuteva, both of which are in clinical validation trials. A third product, Protega, is under development for the prediction of fibrosis and long-term graft failure. Data for these trials are expected to be reported in Q122, with plans in place to commercialise both products quickly afterwards.

Strong need for kidney transplant diagnostics

Globally, approximately 95,000 kidney transplants are performed each year, with an estimated 37–50% of subjects displaying evidence of a post-transplant rejection event. Clinical acute rejection (cAR, 10–15%) occurs in the first year post-transplantation and can be treated with a change in immunosuppressive therapy. Subclinical acute rejection (subAR, 27–40%) or silent rejection usually occurs within one year of transplantation and often goes unnoticed due to the lack of surveillance biopsy programmes in transplant centres. Verici Dx aims to develop tests to understand how a patient’s immune system is likely to respond to organ transplantation and the risk of both cAR and subAR events, as well as long-term damage from fibrosis.

Pre- and post-transplant testing

Verici Dx’s technology is licensed from Mount Sinai and underpinned by the extensive scientific research of Professor Barbara Murphy. Clarava uses blood-based, RNA immunophenotyping to deliver a pre-transplant risk profile of early acute rejection and can provide a tailored immunosuppressive therapy strategy. Clarava is a first-of-its-kind prognostic and, if approved, currently has no competition on the market. The company’s second product, Tuteva, provides real-time, post-transplant prognostics to identify acute cellular rejection, including hard-to-detect subAR. Current post-transplant standards of care focus on identifying organ damage after it has occurred, often through painful and expensive biopsies.

Close to commercialisation

As of January 2022, Clarava and Tuteva have completed testing requirements in clinical validation trials, with results expected to be published in Q122. In preparation for commercialisation, Verici Dx gained a Clinical Laboratory Improvement Amendments certificate of registration in July 2021 to allow its state-of-the-art test labs in Tennessee to start operations if clinical validation results allow commercialisation. In January 2022, Verici Dx also obtained a Current Procedural Terminology code, a key component for US reimbursement, for Clarava and Tuteva. The last reported cash position (December 2021) was $10.3m and management expects to begin generating revenue in 2022, both of which should support further development of the Verici Dx platform..

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Frankfurt +49 (0)69 78 8076 960

Schumannstrasse 34b

60325 Frankfurt

Germany

London +44 (0)20 3077 5700

280 High Holborn

London, WC1V 7EE

United Kingdom

New York +1 646 653 7026

1185 Avenue of the Americas

3rd Floor, New York, NY 10036

United States of America

Sydney +61 (0)2 8249 8342

Level 4, Office 1205

95 Pitt Street, Sydney

NSW 2000, Australia

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Accuracy of content: All information used in the publication of this report has been compiled from publicly available sources that are believed to be reliable, however we do not guarantee the accuracy or completeness of this report and have not sought for this information to be independently verified. Opinions contained in this report represent those of the research department of Edison at the time of publication. Forward-looking information or statements in this report contain information that is based on assumptions, forecasts of future results, estimates of amounts not yet determinable, and therefore involve known and unknown risks, uncertainties and other factors which may cause the actual results, performance or achievements of their subject matter to be materially different from current expectations.

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No personalised advice: The information that we provide should not be construed in any manner whatsoever as, personalised advice. Also, the information provided by us should not be construed by any subscriber or prospective subscriber as Edison’s solicitation to effect, or attempt to effect, any transaction in a security. The securities described in the report may not be eligible for sale in all jurisdictions or to certain categories of investors.

Investment in securities mentioned: Edison has a restrictive policy relating to personal dealing and conflicts of interest. Edison Group does not conduct any investment business and, accordingly, does not itself hold any positions in the securities mentioned in this report. However, the respective directors, officers, employees and contractors of Edison may have a position in any or related securities mentioned in this report, subject to Edison's policies on personal dealing and conflicts of interest.

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Frankfurt +49 (0)69 78 8076 960

Schumannstrasse 34b

60325 Frankfurt

Germany

London +44 (0)20 3077 5700

280 High Holborn

London, WC1V 7EE

United Kingdom

New York +1 646 653 7026

1185 Avenue of the Americas

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United States of America

Sydney +61 (0)2 8249 8342

Level 4, Office 1205

95 Pitt Street, Sydney

NSW 2000, Australia

Frankfurt +49 (0)69 78 8076 960

Schumannstrasse 34b

60325 Frankfurt

Germany

London +44 (0)20 3077 5700

280 High Holborn

London, WC1V 7EE

United Kingdom

New York +1 646 653 7026

1185 Avenue of the Americas

3rd Floor, New York, NY 10036

United States of America

Sydney +61 (0)2 8249 8342

Level 4, Office 1205

95 Pitt Street, Sydney

NSW 2000, Australia

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