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Completed Phase 3 Interventional Results available

The Safety and Efficacy of SYD-101 in Children With Myopia

ClinicalTrials.gov ID: NCT03918915

Public ClinicalTrials.gov record NCT03918915. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 9:45 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-masked, Vehicle-controlled Study to Assess the Safety and Efficacy of SYD-101 Ophthalmic Solution for the Treatment of Myopia in Children

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Myopia, or nearsightedness, is the most common eye disorder, often affecting more than 40% of adults in Europe, Asia and the USA. Severe myopia is associated with an increased risk of developing other eye conditions such as glucoma, cataracts and retinal detachment, which may lead to blindness. Early treatment of myopia in children could help slow the condition and minimize the risk of complications later in life. This study investigates the use of SYD-101, an eye solution, in slowing-down the progression of myopia in children.

Study identification

NCT ID
NCT03918915
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sydnexis, Inc.
Industry
Enrollment
852 participants

Conditions and interventions

Eligibility (public fields only)

Age range
3 Years to 14 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 24, 2019 (Actual)
Primary completion
May 2, 2024 (Actual)
Completion
May 1, 2025 (Actual)
Last update posted
Jul 30, 2026

2019 – 2025

United States locations

U.S. sites
41
U.S. states
22
U.S. cities
38
Facility City State ZIP Site status
Site 143 Irwindale California 91706 —
Site 144 Pasadena California 91105 —
Site 148 San Diego California 92127 —
Site 104 San Diego California 92131 —
Site 110 Santa Barbara California 93110 —
Site 133 Sunnyvale California 94087 —
Site 130 Colorado Springs Colorado 80920 —
Site 100 Fort Collins Colorado 80528 —
Site 102 Danbury Connecticut 06810 —
Site 150 Waterbury Connecticut 06708 —
Site 122 Fort Lauderdale Florida 33309 —
Site 109 Jupiter Florida 33477 —
Site 119 Sweetwater Florida 33182 —
Site 120 Tamarac Florida 33321 —
Site 124 Marietta Georgia 30060 —
Site 116 Chicago Illinois 60616 —
Site 106 Wilmette Illinois 60091 —
Site 135 Indianapolis Indiana 46202 —
Site 131 Munster Indiana 46321 —
Site 137 Pittsburg Kansas 66762 —
Site 138 Bangor Maine 04401 —
Site 123 Boston Massachusetts 02111 —
Site 114 Washington Missouri 63090 —
Site 132 Henderson Nevada 89052 —
Site 139 Albuquerque New Mexico 87109 —
Site 127 Buffalo New York 14209 —
Site 117 Chapel Hill North Carolina 27517 —
Site 121 Raleigh North Carolina 27603 —
Site 105 Fargo North Dakota 58103 —
Site 111 Medford Oregon 97504 —
Site 147 Tigard Oregon 97223 —
Sie 136 Bala-Cynwyd Pennsylvania 19004-1108 —
Site 128 Cranberry Township Pennsylvania 16066 —
Site 108 Charleston South Carolina 29425 —
Site 126 Lakeway Texas 78734 —
Site 142 San Antonio Texas 78215 —
Site 101 San Antonio Texas 78240 —
Site 115 The Woodlands Texas 77380 —
Site 149 Ogden Utah 84403 —
Site 140 Ogden Utah 84405 —
Site 113 Virginia Beach Virginia 23452 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03918915, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 30, 2026 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03918915 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →