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Completed Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT02104388

Public ClinicalTrials.gov record NCT02104388. 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 23, 2026, 2:20 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 SJP-0035 Ophthalmic Solution for Corneal Epithelial Wound Healing in Patients With Moderate to Severe Corneal Epithelial Disorders

Brief summary

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

The purpose of the study is to determine if SJP-0035 ophthalmic solution is effective in promoting corneal epithelial wound healing in conditions associated with corneal epithelial disorders.

Study identification

NCT ID
NCT02104388
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Senju Pharmaceutical Co., Ltd.
Industry
Enrollment
69 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 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 8, 2014 (Actual)
Primary completion
Aug 4, 2015 (Actual)
Completion
Aug 4, 2015 (Actual)
Last update posted
Mar 29, 2021

2014 – 2015

United States locations

U.S. sites
17
U.S. states
10
U.S. cities
17
Facility City State ZIP Site status
Senju Investigational Site Little Rock Arkansas 72205 —
Senju Investigational Site Glendale California 91206 —
Senju Investigational Site Glendora California 91741 —
Senju Investigational Site Huntington Beach California 92647 —
Senju Investigational Site Lancaster California 93534 —
Senju Investigational Site Newport Beach California 92663 —
Senju Investigational Site Pasadena California 91107 —
Senju Investigational Site Petaluma California 94954 —
Senju Investigational Site Santa Maria California 93454 —
Senju Investigational Site Hoffman Estates Illinois 60169 —
Senju Investigational site Edgewood Kentucky 41017 —
Senju Investigational Site Kansas City Missouri 64111 —
Senju Investigational Site Palisades Park New Jersey 07650 —
Senju Investiational Site Rochester New York 14642 —
Senju Investigational Site High Point North Carolina 27262 —
Senju Investigational Site Rapid City South Dakota 57701 —
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 NCT02104388, 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 Mar 29, 2021 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02104388 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →