XORTX Announces Planned FDA IND Submission for XRx-026 Gout Program Using XORLO™, Targeting USD$700M+ U.S. Gout Market Opportunity
XORTX announced a planned Investigational New Drug (IND) application submission to the U.S. FDA in the fourth quarter of 2026 for its XRx-026 gout program. The company said this advances its regulatory path toward a New Drug Application filing for the program.
Why it matters — For XORTX watchers, this announcement signals progress in the company's regulatory timeline for its XRx-026 gout program toward a future FDA filing.