XORTX Reports that Independent Proxy Firm, ISS, Recommends Shareholders Vote for the Share Consolidation ResolutionGlobeNewsWire • 10/12/23
XORTX Submits Orphan Drug Designation Application to the European Medicines Agency (EMA) to Treat Progressive Kidney DiseaseGlobeNewsWire • 08/29/23
XORTX Reminds Shareholders to Vote ahead of the Proxy Voting Deadline for the Company's Upcoming Annual and Special Meeting of ShareholdersGlobeNewsWire • 06/24/23
XORTX Announces 180-Day Extension to Regain Compliance with Nasdaq Minimum Bid Price DeficiencyGlobeNewsWire • 05/24/23
XORTX Announces Receipt of FDA Orphan Drug Designation to Treat Autosomal Dominant Kidney DiseaseGlobeNewsWire • 04/21/23
XORTX Announces Submission of Orphan Drug Designation Request for XRx-008 Program to Treat Autosomal Dominant Kidney DiseaseGlobeNewsWire • 02/01/23
XORTX Announces New Proof of Concept Data in Autosomal Dominant Polycystic Kidney Disease (ADPKD)GlobeNewsWire • 12/08/22
XORTX Announces Completion of Screening and Enrollment in Bridging Pharmacokinetics StudyGlobeNewsWire • 11/28/22
XORTX Announces Receipt of Nasdaq Notification Regarding Minimum Bid Price DeficiencyGlobeNewsWire • 11/25/22
XORTX Completes Positive Pre-Phase 3 Meeting with the US Food and Drug AdministrationGlobeNewsWire • 09/19/22
XORTX Announces Positive Topline Results from Part 2 Pharmacokinetics Bridging StudyGlobeNewsWire • 08/22/22