Status: Ongoing, but not recruiting participants
ClinicalTrials.gov Identifier: NCT02727881
OHR 1601: A Phase III study of Efficacy and Safety of Squalamine Lactate Opthalmic Solution, 0.2% twice daily in subjects with Neovascular AMD.
Condition: Age-Related Macular Degeneration
Study Type: Interventional
Duration: 36 weeks
Eligibility:
For additional information on this study, please click here
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