drugset / Trial / NCT05992922

A Study to Assess the Safety and Efficacy of IC265 Ophthalmic Solution for Dry Eye in Adult Participants

NCT05992922 ↗

Phase 2 Terminated 40 enrolled Iacta Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will evaluate the safety, tolerability and efficacy of IC265 compared to vehicle in participants with signs and symptoms dry eye disease.

Timeline

Start
2023-10-17
Primary completion
2023-12-19
Completion
2023-12-19

Outcome

Outcome not reported

Stopped: “Unexpected adverse events were observed in a subset of patients on drug. In an over abundance of caution the study was terminated. All adverse events resolved with no sequelae.”

Drugs

EvaluationDrugModalityDoseRoute
Subject IC265 Unknown 1 % Other

Indications