CompletedPhase 2NCT02406209
A Safety and Efficacy Study of NS2 in Patients With Anterior Uveitis
Studying Anterior uveitis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Aldeyra Therapeutics, Inc.
- Principal Investigator
- C.Stephen Foster, MD, FACS, FACRMassachusetts Eye Research and Surgery Institution
- Intervention
- NS2(drug)
- Enrollment
- 45 enrolled
- Eligibility
- 18-85 years · All sexes
- Timeline
- 2015 – 2016
Study locations (15)
- Hull Eye Center, Lancaster, California, United States
- Colorado Retina Associates,PC, Golden, Colorado, United States
- Eye Center of Southern Connecticut, Hamden, Connecticut, United States
- Bascom Palmer Eye Institute, Plantation, Florida, United States
- Valley Eye Physicians & Surgeons, Ayer, Massachusetts, United States
- Ophthalmic Consultants of Boston, Boston, Massachusetts, United States
- Massachusetts Eye Research and Surgery Institution (MERSI), Waltham, Massachusetts, United States
- Oakland Ophthalmic Surgery, Birmingham, Michigan, United States
- Lifelong Vision Foundation, Chesterfield, Missouri, United States
- Tauber Eye Center, Kansas City, Missouri, United States
- UNMC Stanley Truhlsen Eye Institute, Omaha, Nebraska, United States
- Metropolitan Eye Research & Surgery Institute, Palisades Park, New Jersey, United States
- Mid-Atlantic Retina, Philadelphia, Pennsylvania, United States
- Houston Eye Associates, Houston, Texas, United States
- Virginia Eye Consultants, Norfolk, Virginia, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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