Clinical trial

Dose Ranging Study to Determine the Safety, Reactogenicity and Immunogenicity of…

NCT00498654 · Avant Immunotherapeutics, Industry · Completed

Key facts

NCT number NCT00498654
Title Dose Ranging Study to Determine the Safety, Reactogenicity and Immunogenicity of Typhoid Fever Vaccine (Ty800) in Healthy Adult Subjects
Official title A Randomized, Double-Blind, Multi-Center, Placebo-Controlled Dose Ranging Study to Determine the Safety, Reactogenicity and Immunogenicity of a Single Oral Dose Typhoid Fever Vaccine (Ty800) in Healthy Adult Subjects
Lead sponsor Avant Immunotherapeutics, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Typhoid Fever
Intervention type Biological
Interventions Ty800 (Salmonella typhi) Oral Vaccine
Enrollment 180
Start date Jul 1, 2007
Primary completion Oct 1, 2007
Completion Jun 1, 2008
First posted Jul 10, 2007
Last update posted Jul 2, 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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