Clinical trial

Safety and Immunogenicity of a Melanoma DNA Vaccine Delivered by Electroporation

NCT00471133 · Ichor Medical Systems Incorporated, Industry · Completed

Key facts

NCT number NCT00471133
Title Safety and Immunogenicity of a Melanoma DNA Vaccine Delivered by Electroporation
Official title A Phase Ia/Ib Study of the Safety and Immunogenicity of a Xenogeneic Tyrosinase DNA Vaccine Melanoma
Lead sponsor Ichor Medical Systems Incorporated, Industry
Collaborators Memorial Sloan Kettering Cancer Center
Status Completed
Phase Phase 1
Study type Interventional
Conditions Melanoma (Skin), Intraocular Melanoma
Intervention type Biological, Device
Interventions Xenogeneic Tyrosinase DNA Vaccine, TriGrid Delivery System for Intramuscular Electroporation
Enrollment 24
Start date Apr 1, 2007
Primary completion May 1, 2010
Completion May 1, 2010
First posted May 9, 2007
Last update posted Jun 7, 2011
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.

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