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Completed Phase 2 Interventional Results available

Safety and Efficacy of SJP-0035 Ophthalmic Solution in Patients With Moderate to Severe Corneal Epithelial Disorders

ClinicalTrials.gov ID: NCT02929823

Public ClinicalTrials.gov record NCT02929823. 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 Jul 22, 2026, 12:12 PM 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 Double-Masked, Randomized, Multicenter, Placebo-Controlled, Parallel-Group Study of SJP-0035 Ophthalmic Solution Compared With Placebo to Assess Safety and Efficacy of Two Dose Concentrations of SJP-0035 Ophthalmic Solution for Corneal Epithelial Wound Healing in Patients With Moderate to Severe Corneal Epithelial Disorders

Study identification

NCT ID
NCT02929823
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Senju Pharmaceutical Co., Ltd.
Industry
Enrollment
130 participants

Conditions and interventions

Interventions

  • High Dose SJP-0035 Ophthalmic Solution Drug
  • Low Dose SJP-0035 Ophthalmic Solution Drug
  • Vehicle of SJP-0035 Ophthalmic solution Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Aug 31, 2016
Primary completion
May 2, 2017
Completion
May 2, 2017
Last update posted
Apr 12, 2021

2016 – 2017

United States locations

U.S. sites
19
U.S. states
10
U.S. cities
19
Facility City State ZIP Site status
Senju Investigational Site Little Rock Arkansas 72205
Senju Investigational Site Glendora California 91741
Senju Investigational Site Lancaster California 93534
Senju Investigational Site Long Beach California 90805
Senju Investigational Site Montebello California 90640
Senju Investigational Site Pasadena California 91107
Senju Investigational Site Santa Ana California 92705
Senju Investigational Site Miami Florida 33143
Senju Investigational Site Hoffman Estates Illinois 60169
Senju Investigational Site Edgewood Kentucky 41017
Senju Investigational Site Louisville Kentucky 40206
Senju Investigational Site Kansas City Missouri 64111
Senju Investigational Site High Point North Carolina 27262
Senju Investigational Site Rapid City South Dakota 57701
Senju Investigational Site Cedar Park Texas 78613
Senju Investigational Site Houston Texas 77030
Senju Investigational Site Irving Texas 75039
Senju Investigational Site Falls Church Virginia 22044
Senju Investigational Site Norfolk Virginia 23502

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02929823, 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 Apr 12, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02929823 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →