CompletedPHASE1, PHASE2NCT05282953

A Phase I/II Dose-escalating Study of the Safety, Tolerability and Efficacy of KIO-301 Administered Intravitreally to Patients With Retinitis Pigmentosa and Choroideremia (ABACUS)

Studying Choroideremia

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Key facts

Sponsor
Kiora Pharmaceuticals, Inc.
Principal Investigator
Robert Casson
Royal Adelaide Hospital
Intervention
KIO-301(drug)
Enrollment
32 enrolled
Eligibility
18-80 years · All sexes
Timeline
20222026

Study locations (3)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT05282953 on ClinicalTrials.gov

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