A Safety and Efficacy Study of MSI-1256F (Squalamine Lactate) To Treat "Wet" Age-Related Macular Degeneration
Stopped early · Phase 2
Conditions studied: Macular Degeneration
In brief
Age-Related Macular Degeneration (AMD) is a degenerative eye disease of the retina that causes a progressive loss of central vision. AMD is the leading cause of legal blindness among adults age 50 or older in the Western world. AMD presents in two different types - "dry" and the more severe "wet" form. Wet AMD is caused by the growth of abnormal blood vessels in the macula. Squalamine lactate is an investigational drug that may prevent the growth of these abnormal blood vessels. This study will test the safety and efficacy of Squalamine in the treatment of AMD.
Key facts
- Study ID
- NCT00089830
- Run by
- Genaera Corporation
- People needed
- 120
- Starts
- 2004-08-01
- Expected to finish
- 2007-05-01
- Last updated by the study team
- 2007-11-28
Who can join
Age: 50 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients with a diagnosis of "wet" age-related macular degeneration
You may not qualify if…
- Prior treatment of "wet" age-related macular degeneration in the affected eye in the past 3 months
Where it is running
- Genaera Corporation — Plymouth Meeting, Pennsylvania, United States
Full record on ClinicalTrials.gov
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