Clinical Trial 46002

Fort Lauderdale, FL 33073


Phase 4 study where patient has severe dry eyes that is not controlled by Cyclosporine (0.05%) (Restasis). Subject enrollment will be classified by evidence of DED. Solution will be used to treat the patient (Cequa), in eahc eye twice a day for twelve weeks. Cequa is expected to show improved benefits and reduction of severe dry eye disease.


1. Must be 18

2. Must provide written consent 

3. Must have a history of clinical diagnosis of DED

4. Must have a total CSF score of over 6 

5. Must have a BCVA at 20/200 or better in both eyes

6. Must be willing to discontinue use of all dry eye therapy 

7. Women of childbearing potential must have a negative urine pregnancy test 

8. Must agree to use contraception 

Qualified Participants May Receive:

1. Financial compensation TBD

2. Information about other studies and treatment for dry eyes 

Available At:

Pinnacle Research Institute
2900 W Cypress Creek Road, Suite #13
Fort Lauderdale, FL 33073
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If you or someone you care for is interested in participating and lives within 50 miles of the location shown, please complete the form below and click 'Submit'

Clinical trials are medical research studies designed to test the safety and/or effectiveness of new investigational drugs, devices, or treatments in humans. These studies are conducted worldwide for a range of conditions and illnesses. Learn more about clinical research and participating in a study at About Clinical Trials.