Efficacy & Safety of RPh201 Treatment in Patients With Previous Nonarteritic Anterior Ischemic Optic Neuropathy (NAION)
Stopped early · Phase 2 · Has a placebo group
Conditions studied: Nonarteritic Anterior Ischemic Optic Neuropathy
In brief
This study is designed as a double-masked, randomized, placebo-controlled, clinical study to evaluate the efficacy and safety of subcutaneous (SC) administration of RPh201 in participants with previous NAION. All participants enrolled in Cohort A of the study will have a documented history of NAION for at least 12 months and at most, five years prior to enrollment. Participants enrolled in Cohort B of the study will have a documented history of NAION for at least 6 months and at most, three years prior to enrollment.
Key facts
- Study ID
- NCT03547206
- Run by
- Regenera Pharma Ltd
- People needed
- 165
- Starts
- 2018-07-10
- Expected to finish
- 2020-09-27
- Last updated by the study team
- 2020-10-12
Who can join
Age: 50 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Byers Eye Institute at Stanford University — Palo Alto, California, United States
- UCLA Doheny Eye Center — Pasadena, California, United States
- The Eye Care Group — Orange, Connecticut, United States
- The Eye Care Group — Waterbury, Connecticut, United States
- Anne Bates Leach Eye Hospital/Bascom Palmer Eye Institute — Miami, Florida, United States
- Emory University — Atlanta, Georgia, United States
- NorthShore Medical Group — Glenview, Illinois, United States
- Bethesda Neurology, LLC — Rockville, Maryland, United States
- Massachusetts Eye and Ear Infirmary — Boston, Massachusetts, United States
- Washington University Ophthalmology — St Louis, Missouri, United States
- New York Eye and Ear Infirmary of Mount Sinai — New York, New York, United States
- Wills Eye Hospital — Philadelphia, Pennsylvania, United States
- Charleston Neuroscience Institute — Ladson, South Carolina, United States
- Neuro-Eye Clinical Trials, Inc. — Houston, Texas, United States
- University of Virginia — Charlottesville, Virginia, United States
Full record on ClinicalTrials.gov
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