Press Releases April 1, 2026

XORTX Confirms Effective Date of Share Consolidation

XORTX Announces Approved Share Consolidation Effective April 6, 2026

By Marcus Reed XRTX
XORTX Confirms Effective Date of Share Consolidation
XRTX

XORTX Therapeutics Inc., a late-stage clinical pharmaceutical company focused on treatments for gout and kidney diseases, has received all necessary approvals from the TSX Venture Exchange and Nasdaq Stock Exchange to implement a share consolidation on a 1-for-5 basis, effective April 6, 2026. The company is advancing several clinical and preclinical programs targeting gout and kidney-related conditions, with ongoing developments in purine metabolism and uric acid reduction therapies.

Key Points

  • XORTX is consolidating its shares at a ratio of one new share for every five old shares, aiming to meet exchange listing requirements and potentially improve liquidity.
  • The company focuses on innovative therapeutic development for gout, progressive kidney disease, acute organ injury, and diabetic nephropathy, with multiple products in clinical or preclinical stages.
  • Share consolidation has been approved by the TSX Venture Exchange and Nasdaq, indicating compliance with regulatory standards for continued listing and trading.

CALGARY, Alberta, April 01, 2026 (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. ("XORTX" or the “Company”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late-stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, announces that, further to its news release of March 26, 2026, the implementation of its share consolidation on the basis of one (1) new common share for every five (5) old common shares (the “Consolidation”) has received all required approvals of the TSX Venture Exchange and Nasdaq Stock Exchange and will occur on April 6, 2026.

About XORTX Therapeutics Inc.

XORTX is a pharmaceutical company with three clinically advanced products in development: 1) our lead program XRx-026 program for the treatment of gout; 2) XRx-008 program for ADPKD; and 3) XRx-101 for acute kidney and other acute organ injury associated with respiratory virus infections. In addition, the Company is developing XRx-225, a pre-clinical stage program for Type 2 diabetic nephropathy. XORTX is working to advance products that target aberrant purine metabolism and xanthine oxidase to decrease or inhibit production of uric acid. At XORTX, we are dedicated to developing medications that improve the quality of life and health of individuals with gout and other important diseases. Additional information on XORTX is available at www.xortx.com.

 For more information, please contact:

Allen Davidoff, CEO Nick Rigopulos, Director of Communicationsadavidoff@xortx.com nick@alpineequityadv.com+1 403 455 7727 +1 617 901 0785   

Forward Looking Statements

This press release contains express or implied forward-looking statements pursuant to applicable securities laws. These forward-looking statements include, but are not limited to, the Company's beliefs, plans, goals, objectives, expectations, assumptions, estimates, intentions, future performance, other statements that are not historical facts and statements identified by words such as "expects", "anticipates", "intends", "plans", "believes", "seeks", "estimates" or words of similar meaning. These forward-looking statements and their implications are based on the current expectations of the management of XORTX only, and are subject to a number of factors and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements. Such risks, uncertainties, and other factors include, but are not limited to, regulatory approvals, such as the TSXV; the ability to complete the Consolidation; the success and timing of our preclinical studies and clinical trials; the performance of third-party manufacturers and contract research organizations; our plans to develop and commercialize our product candidates; our plans to advance research in other kidney disease applications; and, our ability to obtain and maintain intellectual property protection for our product candidates. Except as otherwise required by applicable law and stock exchange rules, XORTX undertakes no obligation to publicly release any revisions to these forward-looking statements to reflect events or circumstances after the date hereof or to reflect the occurrence of unanticipated events. More detailed information about the risks and uncertainties affecting XORTX is contained under the heading “Risk Factors” in XORTX’s Annual Report on Form 20-F filed with the SEC, which is available on the SEC's website, www.sec.gov (including any documents forming a part thereof or incorporated by reference therein), as well as in our reports, public disclosure documents and other filings with the securities commissions and other regulatory bodies in Canada, which are available on www.sedarplus.ca.


Risks

  • Risk of further regulatory hurdles or delays in executing the share consolidation despite current approvals, which could impact stock liquidity and investor confidence.
  • Clinical and preclinical program risks including trial outcomes, regulatory approvals, and manufacturing challenges that could affect the company’s ability to commercialize products.
  • Market risks related to competition in pharmaceutical development for gout and kidney diseases, intellectual property protection challenges, and possible shifts in healthcare policy or funding that could impact future revenues.

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