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Completed Phase 3 Interventional Results available

CHAMP: Study of NVK-002 in Children With Myopia

ClinicalTrials.gov ID: NCT03350620

Public ClinicalTrials.gov record NCT03350620. 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 Sep 2, 2026, 6:57 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 3-Arm Randomized, Double-Masked, Placebo-Controlled, Phase 3 Study of NVK-002 in Children With Myopia

Brief summary

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

Stage 1: To evaluate the safety and efficacy of 2 concentrations of NVK-002 compared to Vehicle (placebo) for slowing the progression of myopia in children over a 3 year treatment period. Stage 2: To observe safety and efficacy in subjects re-randomized to one (1) year of treatment with NVK-002 or Vehicle following 3 years of treatment in children with progressive myopia.

Study identification

NCT ID
NCT03350620
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Vyluma, Inc.
Industry
Enrollment
670 participants

Conditions and interventions

Eligibility (public fields only)

Age range
3 Years to 17 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
Nov 19, 2017
Primary completion
Sep 6, 2022
Completion
Oct 18, 2023
Last update posted
Nov 26, 2024

2017 – 2023

United States locations

U.S. sites
20
U.S. states
16
U.S. cities
20
Facility City State ZIP Site status
Site #009 Tucson Arizona 85711
Site #015 Berkeley California 94720
Site #003 Fullerton California 92831
Site #016 San Diego California 92129
Site #005 Danbury Connecticut 06810
Site #004 Maitland Florida 32751
Site #024 Peoria Illinois 61615
Site #006 Boston Massachusetts 02115
Site #014 St Louis Missouri 63110
Site #002 New York New York 10036
Site #013 Raleigh North Carolina 27603
Site #001 Columbus Ohio 43210
Site #018 Forest Grove Oregon 97116
Site #011 Elkins Park Pennsylvania 19027
Site #017 Lancaster Pennsylvania 17601
Site #008 Memphis Tennessee 38104
Site #007 San Antonio Texas 78240
Site #012 Kirkland Washington 98034
Site #020 Spokane Washington 99204
Site #021 Madison Wisconsin 53705

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 NCT03350620, 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 Nov 26, 2024 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03350620 live on ClinicalTrials.gov.

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