Safety and Efficacy Study of SJP-0035 Ophthalmic Solution in Patients With Moderate to Severe Corneal Epithelial Disorders
NCT02104388 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 69
Last updated 2021-03-29
Summary
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.
Conditions
- Corneal Epithelial Disorders
Interventions
- DRUG
-
SJP-0035 Ophthalmic Solution
- DRUG
-
Vehicle of SJP-0035 Ophthalmic Solution
Sponsors & Collaborators
-
Senju Pharmaceutical Co., Ltd.
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2014-04-08
- Primary Completion
- 2015-08-04
- Completion
- 2015-08-04
Countries
- United States
Study Locations
More Related Trials
-
Efficacy and Safety of SJP-0132 Eye Drops in Chinese Patients With Dry Eye Disease
NCT06717152 ·Status: COMPLETED ·Phase: PHASE3
-
Study to Evaluate the Safety and Efficacy of CSB-001 Ophthalmic Solution 0.1% in Neurotrophic Keratitis Subjects
NCT04909450 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
A Multi-Center Study Subjects With Dry Eye Syndrome
NCT01745887 ·Status: COMPLETED ·Phase: PHASE1
-
ST266 Eyedrops for the Treatment of Persistent Corneal Epithelial Defects
NCT05066698 ·Status: TERMINATED ·Phase: PHASE2
-
A Clinical Trial to Assess the Efficacy and Safety of Subjects With Dry Eye Disease
NCT06389214 ·Status: COMPLETED ·Phase: PHASE3
-
A Multi-Center, Double-Masked, Randomized, Vehicle-Controlled, Parallel-Group Clinical Trial Evaluating the Safety of Reproxalap Ophthalmic Solution in Subjects With Dry Eye Disease
NCT04735393 ·Status: COMPLETED ·Phase: PHASE3
-
A Multi-Center, Randomized, Double Masked, Parallel-Group, Vehicle-Controlled, Clinical Study to Assess the Safety and Efficacy of Reproxalap Ophthalmic Solution in Subjects With Dry Eye Disease
NCT03404115 ·Status: COMPLETED ·Phase: PHASE2
-
Study of SkQ1 as Treatment for Dry-eye Syndrome
NCT03764735 ·Status: COMPLETED ·Phase: PHASE3
-
A Trial to Assess the Safety and Efficacy of Subjects With Dry Eye Disease
NCT06493604 ·Status: COMPLETED ·Phase: PHASE3
-
Exploratory Study of OPC-12759 Ophthalmic Suspension
NCT01493180 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Evaluate the Safety, Tolerability, and Efficacy of A197 in Subjects With Dry Eye Disease
NCT05238597 ·Status: COMPLETED ·Phase: PHASE2
-
A Multi-Center, Randomized, Double-Masked, Parallel-Group, Vehicle-Controlled, Clinical Trial of Reproxalap to Assess the Safety and Efficacy in Subjects With Dry Eye Disease
NCT03916042 ·Status: COMPLETED ·Phase: PHASE2
-
Clinical Study to Investigate the Systemic Exposure, Safety, and Local Tolerability of SJP002 Ophthalmic Solution in Healthy Male Volunteers
NCT02924155 ·Status: COMPLETED ·Phase: PHASE1
-
A Clinical Study Evaluating the Safety and Efficacy of SI-614 Ophthalmic Solution in Patients With Dry Eye.
NCT02205840 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
ST266 Eye Drops for the Treatment of Persistent Corneal Epithelial Defects
NCT03687632 ·Status: COMPLETED ·Phase: PHASE2
-
Treatment of Adenoviral Conjunctivitis With SHP640 Compared to Placebo
NCT02998554 ·Status: TERMINATED ·Phase: PHASE3
-
A Clinical Trial to Assess Subjects With Dry Eye Disease.
NCT04971031 ·Status: COMPLETED ·Phase: PHASE2
-
Treatment of Bacterial Conjunctivitis With SHP640 Compared to PVP-Iodine and Placebo
NCT03004924 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Efficacy Study of Rebamipide 2% Ophthalmic Suspension in Subjects With Dry Eye - Effects on Central Cornea
NCT01057147 ·Status: COMPLETED ·Phase: PHASE2
-
Safety and Efficacy Study of Rebamipide 2% Ophthalmic Suspension in Patients With Dry Eye
NCT01027013 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy and Safety of AJU-S56 in Dry Eye Syndrome Patients
NCT06337981 ·Status: COMPLETED ·Phase: PHASE2
-
To Assess the Safety and Efficacy of R932348 Ophthalmic Solutions in Patients With Keratoconjunctivitis Sicca
NCT01900249 ·Status: COMPLETED ·Phase: PHASE2
-
Study of INS365 Ophthalmic Solution in Subjects With Dry Eye Disease
NCT00403715 ·Status: COMPLETED ·Phase: PHASE3
-
Study of INS365 Ophthalmic Solution in a Controlled Adverse Environment in Patients With Dry Eye
NCT00037661 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Efficacy of TOP1630 for Dry Eye Syndrome
NCT03088605 ·Status: COMPLETED ·Phase: PHASE2