Kiora Pharmaceuticals Receives Clinical Trial Approval for First-in-Human Evaluation of KIO-301 to Restore Vision in Patients with Retinitis PigmentosaNewsfile Corp • 06/27/22
Kiora Pharmaceuticals Receives Nasdaq Notification of Non-Compliance with Listing Rule 5250(c)(1)Newsfile Corp • 05/31/22
Kiora Pharmaceuticals Announces Presentation of KIO-101 Clinical Trial Data at the American Society of Cataract and Refractive Surgery 2022Newsfile Corp • 04/25/22
Kiora Pharmaceuticals to Participate in Maxim Group's 2022 Virtual Growth Conference March 28th - 30thNewsfile Corp • 03/21/22
Kiora Pharmaceuticals Granted Orphan Drug Designation for KIO-301, an Investigational Drug for the Treatment of Retinitis Pigmentosa (RP)Newsfile Corp • 03/18/22
Kiora Pharmaceuticals Announces Participation at 2022 BIO CEO & Investor ConferenceNewsfile Corp • 02/08/22
Kiora Pharmaceuticals Appoints Erin Parsons to its Board of Directors; Stephen From to Retire from BoardNewsfile Corp • 02/01/22
Kiora Pharmaceuticals to Provide 2022 Business Outlook at the H.C. Wainwright Bioconnect Virtual ConferenceNewsfile Corp • 01/05/22
Kiora Pharmaceuticals Appoints David Hollander, MD, MBA, to its Board of DirectorsNewsfile Corp • 12/15/21
Kiora Reports KIO-101 is Safe and Tolerable; Topline Data Supports Advancing KIO-101 to a Phase 2 Study in Patients with Dry Eye DiseaseNewsfile Corp • 12/14/21
Kiora Pharmaceuticals Reports Third Quarter 2021 Financial Results and Provides Business UpdateGlobeNewsWire • 11/15/21
EyeGate is Now Kiora Pharmaceuticals; Provides Update on Company's Sharpened Clinical Development StrategyGlobeNewsWire • 11/08/21