A Study of Safety and the Local Anesthetic Effect of AG-920 Ophthalmic Solution in a Pediatric Population

American Genomics, LLC61 enrolled

Overview

A Phase 3, randomized, active-controlled, study in pediatric subjects. It is designed to evaluate the safety and anesthetic efficacy of one dose of AG-920 ophthalmic solution compared to Proparacaine Hydrochloride Ophthalmic Solution.

A Phase 3, randomized, active-controlled, single-masked, parallel-group design study in pediatric subjects performed in the US. It is designed to evaluate the safety and anesthetic efficacy of one dose of AG-920 compared to Proparacaine. In this study, parent/legal guardians will provide informed consent (and where applicable, subjects will provide assent). Subjects who fulfill all the inclusion criteria and none of the exclusion criteria will be randomized in a 1:1 ratio to receive a single dose of AG 920 or Proparacaine into one (study) eye. Each dose of AG-920 or Proparacaine HCl will consist of two drops in the study eye. After the completion of dosing, subjects will undergo an eye exam, and the ability to conduct that eye exam will be documented. Investigational medicinal product (IMP) dosing will be performed by the study staff.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

SINGLE

Enrollment

Conditions

Anesthesia, Local

Interventions

AG-920DRUG

AG-920 Sterile Topical Ophthalmic Solution

Proparacaine OphthalmicDRUG

0.5% Proparacaine Hydrochloride

Eligibility

Sex: ALLMax age: 10 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: 1. Pre-pubescent with no childbearing potential 2. Capable of undergoing an eye exam 3. Subject's legally appointed and authorized representative willing to sign and date an informed consent form (ICF) and, where appropriate, the subject willing to sign an assent form prior to any study-related procedures being performed. 4. Parent/legal guardian and subject are willing and able to follow instructions and can be present for the required study visits and Follow-up Phone Call for the duration of the study. 5. Have a healthy, normal cornea. Exclusion Criteria: 1. Have participated in an investigational study (drug or device) within the past 30 days. 2. Have a known contraindication to local anesthetics. 3. Children with known autism spectrum disorders or known to have heightened sensitivity. 4. Corneal pathology that would make the corneal sensitivity lower/higher or make the test hard to perform or interpret. 5. Have low visual acuity 6. Manifest nystagmus 7. Have had ocular surgery or general surgery within the past 45 days. 8. Have had an intravitreal injection in either eye within 14 days of randomization. 9. Have ocular surface disease.

Locations (1)

American Genomics Site 2

McAllen, Texas, United States

Outcomes

Primary Outcomes

The Proportion of Participants in Which an Eye Exam Was Able to be Performed

Was the investigator was able to perform the eye examination without additional anesthesia

Time frame: Two to four minutes following treatment (last drop) of IMP

Secondary Outcomes

Number of Participants With Treatment Emergent Adverse Events (TEAEs)

TEAEs will be summarized by treatment group using frequency and percent for each system, organ, class (SOC) and preferred term within each SOC. Summaries will be presented separately for ocular and non-ocular Adverse Events (AEs).

Time frame: From randomization through study completion (up to 4 days following treatment)

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.