A Study of Safety and Efficacy of UNR844 Chloride (UNR844-Cl) Eye Drops in Subjects With Presbyopia.
Completed · Phase 2 · Has a placebo group
Conditions studied: Presbyopia
In brief
The purpose of this study was to assess the effect of topical UNR844-Cl (lipoic acid choline ester chloride) ophthalmic solution on near visual function in presbyopic subjects.
Key facts
- Study ID
- NCT03809611
- Run by
- Novartis Pharmaceuticals
- People needed
- 125
- Starts
- 2019-04-26
- Expected to finish
- 2019-12-16
- Last updated by the study team
- 2022-05-11
Who can join
Age: 45 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Written informed consent must be obtained before any assessment is performed
- Impaired near vision in each eye and when using both eyes, without any near correction
- Need a certain level of near correction
You may not qualify if…
- Impaired distance vision in either eye, with distance correction (if any)
- Severe short- or long-sightedness
- Any significant medical or clinical conditions affecting vision, the eyes or general health
Where it is running
- Novartis Investigative Site — Mission Hills, California, United States
- Novartis Investigative Site — Newport Beach, California, United States
- Novartis Investigative Site — Largo, Florida, United States
- Novartis Investigative Site — Mt. Dora, Florida, United States
- Novartis Investigative Site — Washington, Missouri, United States
- Novartis Investigative Site — Allenwood, Pennsylvania, United States
- Novartis Investigative Site — Cranberry Township, Pennsylvania, United States
- Novartis Investigative Site — Kingston, Pennsylvania, United States
- Novartis Investigative Site — Memphis, Tennessee, United States
- Novartis Investigative Site — Nashville, Tennessee, United States
- Novartis Investigative Site — Nashville, Tennessee, United States
- Novartis Investigative Site — Cedar Park, Texas, United States
- Novartis Investigative Site — Houston, Texas, United States
- Novartis Investigative Site — Norfolk, Virginia, United States
Full record on ClinicalTrials.gov
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