Safety and Efficacy of AGN-199201 and AGN-190584 in Patients With Presbyopia
Completed · Phase 2
Conditions studied: Presbyopia
In brief
A study to evaluate the safety and efficacy of AGN-199201 alone, AGN-190584 alone and concurrent use of AGN-199201 and AGN-190584 in patients with presbyopia (inability to focus for near vision).
Key facts
- Study ID
- NCT02197806
- Run by
- Allergan
- People needed
- 65
- Starts
- 2014-07-01
- Expected to finish
- 2014-11-01
- Last updated by the study team
- 2015-12-03
Who can join
Age: 40 and older, up to 55. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Presbyopia in each eye that impacts daily activities.
You may not qualify if…
- Use of any topical ophthalmic medications, including artificial tears
- Contact lens use in either eye within 14 days or planned use during the study
- History of eye surgery
- Diagnosis of any type of glaucoma or ocular hypertension
Where it is running
- Study site — Newport Beach, California, United States
Full record on ClinicalTrials.gov
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