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Clinical Trials/NCT01551056
NCT01551056
Completed
Phase 3

A Multi-Center, Double-Masked, Randomized, Vehicle-Controlled, Evaluation of the Onset and Duration of Action of Cetirizine 0.24% Ophthalmic Solution (Formula AFH-002) Compared to Vehicle (Formula AFH-001) in the Conjunctival Allergen Challenge (CAC) Model of Acute Allergic Conjunctivitis

Aciex Therapeutics, Inc.1 site in 1 country91 target enrollmentMarch 2012

Overview

Phase
Phase 3
Intervention
AC-170 0.24%
Conditions
Allergic Conjunctivitis
Sponsor
Aciex Therapeutics, Inc.
Enrollment
91
Locations
1
Primary Endpoint
Ocular Itching at Duration of Action (16 Hours + 1 Hour Post-dose)
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the onset and duration of action of AC-170 0.24% compared to vehicle in the prevention of the signs and symptoms of allergic conjunctivitis in the conjunctival allergen challenge (CAC) model.

Registry
clinicaltrials.gov
Start Date
March 2012
End Date
June 2012
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • positive bilateral conjunctival allergen challenge (CAC) reaction

Exclusion Criteria

  • known contraindications or sensitivities to the study medication or its components
  • any ocular condition that, in the opinion of the investigator, could affect the subjects safety or trial parameters
  • use of disallowed medication during the period indicated prior to the enrollment or during the study

Arms & Interventions

AC-170 0.24%

Intervention: AC-170 0.24%

AC-170 0%

Intervention: AC-170 0%

Outcomes

Primary Outcomes

Ocular Itching at Duration of Action (16 Hours + 1 Hour Post-dose)

Time Frame: 3, 5, 7 minutes post-CAC

A treatment efficacy Conjunctival Allergen Challenge (CAC) was performed 16 hours + 1 hour after drop instillation. Ocular itching was assessed by the patient on a 0-4 scale (0=none to 4=severe). Average of ocular itching score over both eyes was analyzed.

Conjunctival Redness at Duration of Action (16 Hours + 1 Hour Post-dose)

Time Frame: 7, 15, 20 minutes post-CAC

A treatment efficacy CAC was performed 16 hours + 1 hour after drop instillation. Conjunctival Redness was assessed by the patient on a 0-4 scale (0=none to 4=severe). Average of conjunctival redness score over both eyes was analyzed.

Conjunctival Redness at Onset of Action (15 Minutes Post-dose)

Time Frame: 7, 15, 20 minutes post-CAC

A treatment efficacy CAC was performed 15 minutes after drop instillation. Conjunctival Redness was assessed by the patient on a 0-4 scale (0=none to 4=severe). Average of conjunctival redness score over both eyes was analyzed.

Ocular Itching at Onset of Action (15 Minutes Post-dose)

Time Frame: 3, 5, 7 minutes post-CAC

A treatment efficacy CAC was performed 15 minutes after drop instillation. Ocular itching was assessed by the patient on a 0-4 scale (0=none to 4=severe). Average of ocular itching score over both eyes was analyzed.

Secondary Outcomes

  • Nasal Congestion at Onset of Action (15 Minutes Post-dose)(7, 15, 20 minutes post-CAC)
  • Ciliary Redness at Duration of Action (16 Hours + 1 Hour Post-dose)(7, 15, 20 minutes post-CAC)
  • Episcleral Redness at Duration of Action (16 Hours + 1 Hour Post-dose)(7, 15, 20 minutes post-CAC)
  • Eyelid Swelling at Duration of Action (16 Hours + 1 Hour Post-dose)(7, 15, 20 minutes post-CAC)
  • Eyelid Swelling at Onset of Action (15 Minutes Post-dose)(7, 15, 20 minutes post-CAC)
  • Number of Participants With At Least One of the Nasal Symptoms Present (Rhinorrhea + Nasal Pruritus + Ear or Palate Pruritus + Nasal Congestion) at Duration of Action (16 Hours + 1 Hour Post-dose)(7, 15, 20 minutes post-CAC)
  • Number of Participants With At Least One of the Nasal Symptoms Present (Rhinorrhea + Nasal Pruritus + Ear or Palate Pruritus + Nasal Congestion) at Onset of Action (15 Minutes Post-dose)(7, 15, 20 minutes post-CAC)
  • Chemosis at Duration of Action (16 Hours + 1 Hour Post-dose)(7, 15, 20 minutes post-CAC)
  • Rhinorrhea at Duration of Action (16 Hours +1 Hour Post-dose)(7, 15, 20 minutes post-CAC)
  • Ear or Palate Pruritis at Onset of Action (15 Minutes Post-dose)(7, 15, 20 minutes post-CAC)
  • Ciliary Redness at Onset of Action (15 Minutes Post-dose)(7, 15, 20 minutes post-CAC)
  • Rhinorrhea at Onset of Action (15 Minutes Post-dose)(7, 15, 20 minutes post-CAC)
  • Nasal Pruritis at Onset of Action (15 Minutes Post-dose)(7, 15, 20 minutes post-CAC)
  • Nasal Congestion at Duration of Action (16 Hours + 1 Hour Post-dose)(7, 15, 20 minutes post-CAC)
  • Tolerability of Study Medication at Visit 3A(upon instillation, 1 minute and 2 minutes post instillation)
  • Episcleral Redness at Onset of Action (15 Minutes Post-dose)(7, 15, 20 minutes post-CAC)
  • Chemosis at Onset of Action (15 Minutes Post-dose)(7, 15, 20 minutes post-CAC)
  • Tearing at Duration of Action (16 Hours + 1 Hour Post-dose)(7, 15, 20 minutes post-CAC)
  • Tearing at Onset of Action (15 Minutes Post-dose)(7, 15, 20 minutes post-CAC)
  • Nasal Pruritis at Duration of Action (16 Hours + 1 Hour Post-dose)(7, 15, 20 minutes post-CAC)
  • Ear or Palate Pruritis at Duration of Action (16 Hours + 1 Hour Post-dose)(7, 15, 20 minutes post-CAC)

Study Sites (1)

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