Clinical trial

MSI-1256F (Squalamine Lactate) in Combination With Verteporfin in Patients With…

NCT00094120 · Genaera Corporation, Industry · Terminated

Key facts

NCT number NCT00094120
Title MSI-1256F (Squalamine Lactate) in Combination With Verteporfin in Patients With "Wet" Age-Related Macular Degeneration (AMD)
Official title Safety and Efficacy of MSI-1256F (Squalamine Lactate) in Combination With Verteporfin in Patients With "Wet" Age-Related Macular Degeneration (AMD)
Lead sponsor Genaera Corporation, Industry
Status Terminated
Phase Phase 2
Study type Interventional
Conditions Macular Degeneration
Intervention type Drug
Interventions MSI-1256F (Squalamine Lactate)
Enrollment 60
Start date Oct 1, 2004
Primary completion Feb 1, 2007
Completion Feb 1, 2007
First posted Oct 14, 2004
Last update posted Jan 9, 2008
Countries United States

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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