Clinical trial

Safety and Tolerability of Intravitreal VEGF Trap Formulations in Subjects With…

NCT00383370 · Regeneron Pharmaceuticals, Industry · Completed

Key facts

NCT number NCT00383370
Title Safety and Tolerability of Intravitreal VEGF Trap Formulations in Subjects With Neovacular AMD
Official title A Trial to Assess the Safety and Tolerability of Repeated Doses of Intravitreal Administration of Two VEGF Trap Formulations in Subjects With Neovascular Age Related Macular Degeneration
Lead sponsor Regeneron Pharmaceuticals, Industry
Status Completed
Phase Phase 1
Study type Interventional
Conditions Neovascular Age Related Macular Degeneration
Intervention type Biological, Drug
Interventions VEGF Trap
Enrollment 20
Start date Oct 1, 2006
Primary completion Sep 1, 2007
Completion Jul 1, 2008
First posted Oct 3, 2006
Last update posted Apr 21, 2011
Countries United States

At a glance

  • No Results posted
  • None Linked FDA submissions

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

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

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

Browse all ClinicalTrials.gov studies