drugset / Trial / NCT01438281

Study to Evaluate the Ocular Tolerance of SYL1001 in Healthy Volunteers

NCT01438281 ↗

Phase 1 Completed 30 enrolled Sylentis, S.A.
NaSingle-groupSingle-blindTreatment

Summary

The purpose of this study is to determine whether SYL1001 is safe for the prevention and treatment of ocular pain and dry eye syndrome.

Timeline

Start
2011-07
Primary completion
2011-11
Completion
2012-06

Outcome

Met primary endpoint

paper These trials achieved their primary endpoints of identifying the most effective dose of SYL1001 (1.125%). PMID 27893109 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject SYL1001 Small interfering RNA (siRNA) — Topical

Indications