Clinical Trials Directory

Trials / Terminated

TerminatedNCT00094120

MSI-1256F (Squalamine Lactate) in Combination With Verteporfin in Patients With "Wet" Age-Related Macular Degeneration (AMD)

Safety and Efficacy of MSI-1256F (Squalamine Lactate) in Combination With Verteporfin in Patients With "Wet" Age-Related Macular Degeneration (AMD)

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
60 (planned)
Sponsor
Genaera Corporation · Industry
Sex
All
Age
50 Years
Healthy volunteers
Not accepted

Summary

Age-Related Macular Degeneration (AMD) is a degenerative 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 when administered with verteporfin therapy in patients with "wet" AMD.

Conditions

Interventions

TypeNameDescription
DRUGMSI-1256F (Squalamine Lactate)

Timeline

Start date
2004-10-01
Primary completion
2007-02-01
Completion
2007-02-01
First posted
2004-10-14
Last updated
2008-01-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00094120. Inclusion in this directory is not an endorsement.

MSI-1256F (Squalamine Lactate) in Combination With Verteporfin in Patients With "Wet" Age-Related Macular Degeneration ( (NCT00094120) · Clinical Trials Directory