A Study of RX-10045 in the Treatment of Dry Eye Disease
Completed · Phase 2 · Has a placebo group
Conditions studied: Dry Eye Syndrome
In brief
The primary purpose of this study is to assess the efficacy, tolerability and safety of RX-10045 Ophthalmic Solution in patients with Dry Eye Disease.
Key facts
- Study ID
- NCT01675570
- Run by
- C.T. Development America, Inc.
- People needed
- 150
- Starts
- 2012-08-01
- Expected to finish
- 2012-11-01
- Last updated by the study team
- 2013-02-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Have a patient reported history of dry eye in both eyes
- Presence of dry eye symptoms
- Presence of dry eye signs, destabilized tear film break-up time and corneal staining
You may not qualify if…
- Known contraindications or sensitivities to study medication or its components
- Any ocular condition that, in the opinion of the investigator, could affect the subject's safety or trial parameters
- Use of disallowed medication during the period indicated prior to the enrollment or during the study
- Be a female who is currently pregnant, planning a pregnancy, lactating, or not using a medically acceptable form of birth control
Where it is running
- Andover Eye Associates — Andover, Massachusetts, United States
Full record on ClinicalTrials.gov
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