Clinical trial

Study of Reactogenicity, Safety, Immunogenicity, and Pock Lesion Formation of a…

NCT00042094 · DynPort Vaccine Company LLC, A GDIT Company, Industry · Completed

Key facts

NCT number NCT00042094
Title Study of Reactogenicity, Safety, Immunogenicity, and Pock Lesion Formation of a Cell-Cultured Smallpox Vaccine Compared to Dryvax®
Official title A Phase 1 Study of Reactogenicity, Safety, Immunogenicity, and Pock Lesion Formation (Take Rate) of a Cell-Cultured Smallpox Vaccine (CCSV) Compared to a Calf Lymph Vaccine (Dryvax®)
Lead sponsor DynPort Vaccine Company LLC, A GDIT Company, Industry
Status Completed
Phase Phase 1
Study type Interventional
Conditions Smallpox
Intervention type Biological
Interventions Cell-Cultured Smallpox Vaccine compared to Dryvax®
Enrollment 350
Start date Mar 1, 2002
Completion Mar 1, 2003
First posted Jul 26, 2002
Last update posted Jun 30, 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.

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

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