CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 101 enrolled
Drug / intervention
AC-170 0.05% +3 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01332188
NCT01332188Phase 3Completed

A Single Center, Double-Masked, Randomized, Vehicle-Controlled, Parallel-Group Study Evaluating the Efficacy of Three Different Concentrations of Cetirizine (0.05%, 0.1%, and 0.24%) Ophthalmic Solution Versus Vehicle in the Treatment of Allergic Conjunctivitis in the Conjunctival Allergen Challenge Model (CAC)

Aciex Therapeutics, Inc.·interventional·Posted Apr 11, 2011·Updated Aug 30, 2017

In Brief

A Phase 3 clinical trial evaluating AC-170 0.05%, AC-170 0.1%, and 2 other interventions for Allergic Conjunctivitis. Completed, enrolled 101 participants across 1 site.

Detailed Summary

The purpose of this study is to evaluate the efficacy of different concentrations of AC-170 compared to vehicle in the prevention of the signs and symptoms of allergic conjunctivitis in the conjunctival allergen challenge (CAC) Model.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 3CompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedApr 11, 2011
Enrollment StartApr 1, 2011
Primary CompletionJun 1, 2011
Study CompletionOct 1, 2011
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 15.2 years ago

Interventions

AC-170 0.05%drug

1 drop in each eye at 3 separate times during a 21 day period

AC-170 0.1%drug

1 drop in each eye at 3 separate times during a 21 day period

AC-170 0.24%drug

1 drop in each eye at 3 separate times during a 21 day period

AC-170 0%drug

1 drop in each eye at 3 separate times during a 21 day period