Status:
COMPLETED
Study of Brimonidine Tartrate Nanoemulsion Eye Drop Solution in the Treatment of Dry Eye Disease (DED)
Lead Sponsor:
Ocugen
Conditions:
Dry Eye
Eligibility:
All Genders
18+ years
Phase:
PHASE3
Brief Summary
This study evaluates the use of Brimonidine tartrate nanoemulsion eye drop solution in the treatment of Dry Eye Disease (DED). Half of participants will receive Brimonidine and half will receive ophth...
Detailed Description
Dry eye disease (DED) is a common ocular disorder involving the aberrant production and instability of tear film, which results in damage to the ocular surface and is correlated with symptoms of ocula...
Eligibility Criteria
Inclusion
- Aged 18 years or older.
- Sign and date informed consent form approved by the IRB
- History of Dry Eye Disease for ≥6 months
- Demonstrate the following 2 signs of DED in the same eye at Screening and Baseline (Day 1):
- Conjunctival staining at ≥3 (out of a possible score of 6 per eye), and
- Schirmer test (with anesthesia) at ≥1 to ≤7mm in 5 minutes
- Symptomatic evidence of DED by having a global symptom score (Overall SANDE) ≥40 mm at Screening and Baseline (Day 1) visit
- Intraocular pressure (IOP) ≥ 5 mmHg and ≤22 mmHg in each eye
- Women who satisfy one of the following:
- 8a. Are of child-bearing potential (WOCP) who are not pregnant or lactating and who are either abstinent or sexually active on an acceptable method of birth control for at least 4 weeks prior to Visit 1 and throughout the study (i.e., until Day 28), OR 8b. Are post-menopausal or have undergone a sterilization procedure
Exclusion
- Allergic to brimonidine or any similar products, or excipients of brimonidine
- Use of contact lenses within 14 days prior to Screening visit or planned use during study
- Currently receiving brimonidine or other treatment for glaucoma or ocular hypertension or history of glaucoma surgery.
- Receiving or have received any experimental or investigational drug or device within 30 days prior to Screening visit
- Intraocular pressure \<5 mmHg or \>22 mmHg in either eye
- Active ocular infection or history of ocular herpetic keratitis
- History of neurotrophic keratitis or ocular neuropathic pain
- Any history of eyelid surgery or intraocular/ocular surgery within the past 3 months
- Punctal occlusion within 3 months prior to Screening visit or during study
- Corneal epithelial defect larger than 1 mm2 in either eye
- Have active drug/alcohol dependence or abuse history
- Are neonates, pregnant/lactating women, children, or others who may be considered vulnerable populations
- Received corticosteroid-containing eye drops within 14 days prior to Screening visit or planned use during study
- Any change in systemic corticosteroids/immunosuppressives, cyclosporine ophthalmic emulsion 0.05% (Restasis®), cyclosporine ophthalmic solution 0.09% (Cequa™), or lifitegrast ophthalmic solution 5% (Xiidra®) within 30 days prior to Screening visit or planned change during study
- In the opinion of Investigator or Study Coordinator, be unwilling or unable to comply with study protocol or unable to successfully instill eye drops
- Disease, condition, or disorder that in the judgement of Investigator could confound study assessments or limit compliance to study protocol
Key Trial Info
Start Date :
December 3 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 25 2019
Estimated Enrollment :
252 Patients enrolled
Trial Details
Trial ID
NCT03785340
Start Date
December 3 2018
End Date
February 25 2019
Last Update
July 18 2022
Active Locations (16)
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1
Aesthetic Eye Care Institute/David Wirta, MD and Associates
Newport Beach, California, United States, 92663
2
Martel Medical Eye Group
Rancho Cordova, California, United States, 95670
3
Rand Eye Institute
Pompano Beach, Florida, United States, 33064
4
Chicago Cornea Consultants
Hoffman Estates, Illinois, United States, 60169