CompletedPHASE1, PHASE2NCT02309385
Safety and Efficacy Study of DSP-Visulex for the Treatment of 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
- Aciont Inc
- Principal Investigator
- William I Higuchi, PhD, SLPAciont Inc
- Intervention
- 8% Dexamethasone Sodium Phosphate - Visulex(drug)
- Enrollment
- 44 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2014 – 2017
Study locations (6)
- Massachusetts Eye Research and Surgery Institution (MERSI), Cambridge, Massachusetts, United States
- Charlotte Eye, Ear, Nose, and Throat Associates, Charlotte, North Carolina, United States
- Bergstrom Eye Research, Fargo, North Dakota, United States
- B-Berger and Associates, Austin, Texas, United States
- Retina and Uveitis Consultants of Texas, San Antonio, Texas, United States
- Moran Eye Center, University of Utah, Salt Lake City, Utah, United States
Collaborators
National Eye Institute (NEI)
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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