Phase 2
Completed N=130
Safety and Efficacy of SJP-0035 Ophthalmic Solution in Patients With Moderate to Severe Corneal Epithelial Disorders
Corneal Epithelial Disorders
Source: ClinicalTrials.gov NCT02929823 ↗
Enrolled (actual)
130
Serious AEs
0.8%
Results posted
Jun 2018
Primary outcomePrimary: Number of Participants With Clearing of Corneal Fluorescein Staining at Week 5 at Week 5 — 5; 7; 12 Participants
Summary
The purpose of this study is to determine whether SJP-0035 ophthalmic solution is effective in promoting corneal epithelial wound healing in conditions associated with corneal epithelial disorders.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants With Clearing of Corneal Fluorescein Staining at Week 5 at Week 5 |
5; 7; 12 | — |
Eligibility Criteria
Inclusion Criteria
- Is capable of understanding the written informed consent form (ICF), provides signed and witnessed written ICF, and agrees to comply with protocol requirements, including all required study visits
- Is a male or female 18 years of age or older
- Has a moderate to severe corneal epithelial disorder in both eyes
- Has blurred vision caused by corneal epithelial disorders in both eyes at Screening and Randomization
- Is a female of childbearing potential with a negative pregnancy test result at Screening and Randomization and agrees to use effective contraception throughout the study, or is a postmenopausal woman with a negative pregnancy test result at Screening and Randomization
Exclusion Criteria
- Has any corneal stromal or endothelial abnormalities including an active bacterial or viral ocular infection, bullous keratopathy, chemical burns, or any trauma to the cornea in either eye at Screening and Randomization
- Has any active or chronic allergic, bacterial, or viral infection of ocular adnexa and eye structures in either eye at Screening and Randomization
- Has had intraocular surgery (including cataract or vitreous) in either eye within the last 30 days prior to the first dose of study drug
- Has had refractive surgery (including ocular surface laser surgery) in either eye within the last 6 months prior to the first dose of study drug
- Has used any ocular medication (except mydriatics, stain, and topical anesthesia used for study assessments) in either eye within 14 days prior to the first dose of study drug, or is anticipated to require such medications during the study.
- Is a contact lens wearer and cannot discontinue use in both eyes from Screening through EOS
Data sourced from ClinicalTrials.gov (NCT02929823). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.