drugset / Trial / NCT07640867

RCI001 Eye Drops 0.25% in Healthy Adult Male Participants

NCT07640867 ↗

Phase 1 Completed 40 enrolled Rudacure
RandomizedSequentialQuadruple-blindTreatment

Summary

This study is being conducted to evaluate the safety, tolerability, and pharmacokinetics of RCI001 eye drops 0.25% in healthy adult male participants. Pharmacokinetics means how the study drug is absorbed, distributed, and eliminated from the body over time. Participants who meet the study requirements will be randomly assigned to receive either RCI001 eye drops 0.25% or placebo eye drops. The study treatment will be administered to the left eye according to the assigned dosing schedule. The study includes single-dose administration schedules and multiple-dose administration schedules for up to 15 days. The study will monitor safety and tolerability through adverse event assessments, vital signs, physical examinations, electrocardiograms, laboratory tests, eye symptom assessments, and ophthalmic examinations. Blood samples will be collected at scheduled time points to measure the concentration of RCI001 in the blood. Approximately 40 healthy adult male participants are planned to take part in this study.

Timeline

Start
2024-10-28
Primary completion
2025-08-29
Completion
2025-09-20

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject RCI001 Unknown 0.25 % Other

Indications