RecruitingPhase 2NCT06825702

Safety, Tolerability and Efficacy of Intravitreal KIO-104 in Patients With Macular Edema

A Phase 2, Open-label, Multiple Dose Study of the Safety, Tolerability and Efficacy of Intravitreal KIO-104 in Patients With Macular Edema (KLARITY-1)


Sponsor

Kiora Pharmaceuticals, Inc.

Enrollment

28 participants

Start Date

May 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This is a multi-center, open label study to assess the safety, tolerability, and efficacy of KIO-104 administered by IVT injection to the study eye of eligible participants with macular edema.


Eligibility

Min Age: 18 YearsMax Age: 85 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called KIO-104 for people with macular edema. The study is currently recruiting participants at 6 locations. People eligible for this study include aged 18 Years to 85 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGKIO-104

KIO-104 is an ophthalmic formulation for IVT injection of the active pharmaceutical ingredient (API) KIO-100, a novel, non-steroidal, small molecule inhibitor of dihydroorotate dehydrogenase (DHODH).


Locations(6)

Sydney Eye Hospital

Sydney, New South Wales, Australia

Sydney West Retina

Westmead, New South Wales, Australia

Royal Adelaide Hospital

Adelaide, South Australia, Australia

Hobart Eye Surgeons

Hobart, Tasmania, Australia

Centre for Eye Research Australia

East Melbourne, Victoria, Australia

Lions Eye Institute Limited

Nedlands, Western Australia, Australia

View Full Details on ClinicalTrials.gov

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NCT06825702


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