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Exagen Inc. Announces New PLA Code and Medicare Pricing for Proprietary AVISE® Lupus Test

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Exagen Inc. (Nasdaq: XGN) announced that Noridian, a Medicare Administrative Contractor, has established pricing for AVISE® Lupus following the approval of the PLA code 0312U by the AMA. Effective April 1, 2022, this code signifies the test's proprietary nature, combining Cell-Bound Complement Activation Products (CB-CAPs) with an SLE-likelihood assessment. CEO Ron Rocca emphasized that this milestone enhances accessibility to AVISE Lupus, promoting better autoimmune disease diagnosis.

Positive
  • Noridian's pricing for AVISE Lupus indicates recognition of its value and novel technology.
  • Approval of PLA code 0312U enhances the test's credibility and potential market acceptance.
Negative
  • Potential risks exist regarding Medicare coverage and reimbursement for AVISE Lupus.
  • Market acceptance is not guaranteed and depends on third-party payor decisions.

SAN DIEGO, May 11, 2022 (GLOBE NEWSWIRE) -- Exagen Inc. (Nasdaq: XGN), a leading provider of autoimmune testing solutions, announced today that Medicare Administrative Contractor (MAC) Noridian has provided pricing for AVISE® Lupus. Noridian’s decision to price AVISE Lupus follows the approval by the American Medical Association (AMA) CPT® Editorial Panel of Proprietary Laboratory Code (PLA) code 0312U for AVISE Lupus. The PLA code has an effective date of April 1, 2022.  

Noridian’s pricing of AVISE Lupus along with AMA CPT’s issuance of PLA Code 0312U both reflect the proprietary and novel aspects of AVISE Lupus which combine Cell-Bound Complement Activation Products (CB-CAPs) along with an algorithmic SLE-likelihood assessment to aid providers in the evaluation of suspected SLE patients.

Ron Rocca, President and CEO of Exagen Inc. shared, “being the recipient of this dedicated PLA code marks an important milestone for Exagen. This code showcases the importance of our test and is a step forward in our commitment to making AVISE Lupus, as well as the rest of our tests, accessible to everyone who needs it.”

About Exagen Inc.

Exagen is dedicated to transforming the care continuum for patients suffering from debilitating and chronic autoimmune diseases by enabling timely differential diagnosis and optimizing therapeutic intervention. Exagen has developed and is commercializing a portfolio of innovative testing products under its AVISE® brand, several of which are based on our proprietary Cell-Bound Complement Activation Products, or CB-CAPs, technology. Exagen’s goal is to enable providers to improve care for patients through the differential diagnosis, prognosis, and monitoring of complex autoimmune and autoimmune-related diseases, including rheumatoid arthritis and lupus.

For more information, please visit Exagen.com and follow @ExagenInc on Twitter.

Forward Looking Statements

Exagen cautions you that statements in this press release regarding matters that are not historical facts are forward-looking statements. These statements are based on Exagen's current beliefs and expectations. Such forward-looking statements include, but are not limited to, statements regarding the receipt of a PLA code, related implications and judgements regarding Exagen’s products presented in this release and pricing from Medicare is not meant to imply that AVISE Lupus and AVISE CTD are in-network covered benefits under Medicare. Furthermore, commercial payors are under no obligation to recognize a PLA code or to reimburse at the Medicare rate. The inclusion of forward-looking statements should not be regarded as a representation by Exagen that any of its plans will be achieved. Actual results may differ from those set forth in this press release due to the risks and uncertainties inherent in Exagen’s business, including, without limitation: the COVID-19 pandemic may continue to adversely affect its business, financial condition and results of operations, including as a result of slowdown in its operations as well as those of its suppliers and courier services, impeding patient movement and interruptions to healthcare services causing a decrease in test volumes, disruptions to the supply chain of material needed for its tests causing an increase in cost per test, its sales and commercialization activities and its ability to receive specimens and perform or deliver the results from its tests, delays in reimbursement and coverage decisions from Medicare and third-party payors, including potential negative coverage decisions on Medicare regarding AVISE Lupus, and in interactions with regulatory authorities, and delays in ongoing and planned clinical trials involving its tests; Exagen’s commercial success depends upon attaining and maintaining significant market acceptance of its testing products and promoted therapeutics among rheumatologists, patients, third-party payors and others in the medical community; Exagen’s ability to successfully execute on its business strategies; third-party payors not providing coverage and adequate reimbursement for Exagen’s testing products or promoted therapeutics, including Exagen’s ability to collect funds due based on pricing of the new PLA code; Exagen’s ability to obtain and maintain intellectual property protection for its testing products; regulatory developments affecting Exagen’s business; and other risks described in Exagen’s prior press releases and Exagen’s filings with the Securities and Exchange Commission (“SEC”), including under the heading “Risk Factors” in Exagen’s Annual Report on Form 10-K for the year ended December 31, 2021 and any subsequent filings with the SEC. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof, and Exagen undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date hereof. All forward-looking statements are qualified in their entirety by this cautionary statement, which is made under the safe harbor provisions of the Private Securities Litigation Reform Act of 1995.

Investor Relations
Exagen Inc.
Ryan Douglas
rdouglas@exagen.com 
760.560.1525

Company
Exagen Inc.
Kamal Adawi, Chief Financial Officer
kadawi@exagen.com
760.477.5514


FAQ

What is the significance of PLA code 0312U for Exagen's AVISE Lupus test?

The PLA code 0312U indicates the proprietary nature of the AVISE Lupus test and supports its pricing by Medicare.

When did Noridian's pricing for AVISE Lupus take effect?

Noridian's pricing for AVISE Lupus took effect on April 1, 2022.

What are the implications of Noridian pricing for Exagen Inc. (XGN)?

Noridian's pricing could enhance revenue potential for Exagen by increasing test accessibility and market recognition.

How might Medicare coverage decisions impact Exagen's AVISE Lupus test?

Medicare coverage decisions may affect reimbursement rates, impacting Exagen's revenue and test adoption.

What challenges could Exagen face after receiving the PLA code for AVISE Lupus?

Exagen may encounter challenges in market acceptance and reimbursement from third-party payors post-PLA code approval.

Exagen Inc.

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