XORTX Highlights Genetic Links to High Uric Acid and Gout in New Research
Written by Emily J. Thompson, Senior Investment Analyst
Updated: 1h ago
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Source: Newsfilter
- Genetic Research Breakthrough: XORTX's recent findings indicate that a clinical study involving 2.6 million individuals identified 410 genetic factors linked to gout, including 149 new discoveries, which further supports the company's treatment strategy for hyperuricemia.
- Drug Development Potential: CEO Allen Davidoff emphasized that targeting xanthine oxidase (XO) for drug development holds significant therapeutic potential, particularly for patients with diabetic and non-diabetic kidney diseases, potentially paving the way for personalized treatment approaches.
- Board Changes: XORTX appointed Krysta Davies Foss as a new director, enhancing the company's strategic leadership in biotechnology, which is expected to drive the advancement of clinical programs and long-term growth strategies.
- Financing Update: The company clarified previous financing details, confirming the issuance of 1.75 million common shares and pre-funded warrants, raising a total of $1.1 million, reflecting the company's active engagement in capital markets.
Analyst Views on XRTX
About XRTX
XORTX Therapeutics Inc. is a pharmaceutical company. The Company is engaged in developing medications that improve the quality of life and health of individuals with gout and other important diseases. It has three clinically advanced products in development: its lead program, XRx-026 program for the treatment of gout; XRx-008 program for autosomal dominant polycystic kidney disease (ADPKD); and 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 II diabetic nephropathy. It is working to advance products that target aberrant purine metabolism and xanthine oxidase to decrease or inhibit the production of uric acid. The XRx-026 program is designed to decrease the chronically high serum uric acid concentration in the blood (SUA) by inhibiting the production of uric acid by the xanthine oxidase enzyme by administering a xanthine oxidase inhibitor-oxypurinol.
About the author

Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.





