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
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Kiora Pharmaceuticals, Inc.
- Principal Investigator
- Robert CassonRoyal Adelaide Hospital
- Intervention
- KIO-301(drug)
- Enrollment
- 32 enrolled
- Eligibility
- 18-80 years · All sexes
- Timeline
- 2022 – 2026
Study locations (3)
- Save Sight Institute, Sydney, New South Wales, Australia
- Royal Adelaide Hospital, Adelaide, South Australia, Australia
- Harley Eye Clinic, North Adelaide, South Australia, Australia
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.govOther trials for Choroideremia
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