Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Terminated Phase 3 Interventional

A Safety and Efficacy Study of Squalamine Lactate for Injection (MSI-1256F) for "Wet" Age-Related Macular Degeneration

ClinicalTrials.gov ID: NCT00139282

Public ClinicalTrials.gov record NCT00139282. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 26, 2026, 10:06 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Multicenter, Randomized, Double-Masked, Controlled Study of Squalamine Lactate (MSI-1256F) for Injection for the Treatment of Subfoveal Choroidal Neovascularization Associated With Age-Related Macular Degeneration

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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 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 evaluate the safety and efficacy of Squalamine lactate in the treatment of AMD in patients, the exact number of which will be determined based on data from the sponsor's ongoing Phase 2 trials. The trial objective is to evaluate the safety and efficacy of two doses of Squalamine lactate for Injection administered as intravenous infusions weekly for 4 weeks followed by maintenance doses every 4 weeks through week 104 compared with the safety and efficacy in the control group.

Study identification

NCT ID
NCT00139282
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Genaera Corporation
Industry
Enrollment
Not listed

Conditions and interventions

Eligibility (public fields only)

Age range
50 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 2005 (Type not available)
Primary completion
Not listed
Completion
Not listed
Last update posted
Nov 28, 2007

Started 2005

United States locations

U.S. sites
29
U.S. states
17
U.S. cities
27
Facility City State ZIP Site status
Retina-Vitreous Associates Medical Group Beverly Hills California 90211 —
Eldorado Retina Associates Louisville Colorado 80027 —
Florida Eye Microsurgical Institute Boynton Beach Florida 33426 —
National Ophthalmic Research Institute Fort Myers Florida 33912 —
University of Florida Jacksonville Florida 32256 —
Magruder Eye Institute Orlando Florida 32803 —
East Florida Eye Institute Stuart Florida 34994 —
Retina Associates of Florida Tampa Florida 33609 —
Center for Retina and Macular Disease Winter Haven Florida 33880 —
Midwest Eye Institute Indianapolis Indiana 46280 —
Retina Associates, PA Shawnee Mission Kansas 66204 —
Cumberland Valley Retina Consultants, PC Hagerstown Maryland 21740 —
Delaware Valley Retina Associates Lawrenceville New Jersey 08648 —
Retina Associates of New Jersey Teaneck New Jersey 07666 —
MaculaCare New York New York 10021 —
Charlotte Eye, Ear, Nose & Throat Associates Charlotte North Carolina 28210 —
Horizon Eye Care Charlotte North Carolina 28211 —
The Ohio State University, Havener Eye Institute Columbus Ohio 43210 —
Penn State Ophthalmology Hershey Pennsylvania 17033 —
Retina Vitreous Consultants Pittsburgh Pennsylvania 15213 —
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15213 —
Genaera Corporation Plymouth Meeting Pennsylvania 19462 —
Carolina Retina Center Columbia South Carolina 29223 —
Black Hills Regional Eye Institute Rapid City South Dakota 57701 —
Southeastern Retina Associates Kingsport Tennessee 37660 —
Retina Research Center Austin Texas 78705 —
Garcia & Associates, MD, PA Houston Texas 77002 —
John Moran Eye Center Salt Lake City Utah 84132 —
Virginia Retina Center Leesburg Virginia 20176 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00139282, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 28, 2007 · Synced Oct 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00139282 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →