Clinical trial

A Phase 2 Study of Immunogenicity, Safety and Tolerability of CSL412 in Elderly…

NCT00479648 · Seqirus, Industry · Completed

Key facts

NCT number NCT00479648
Title A Phase 2 Study of Immunogenicity, Safety and Tolerability of CSL412 in Elderly Participants
Official title A Phase II, Double-Blind, Randomised, Controlled, Multi-Centre Study to Evaluate the Immunogenicity, Safety and Tolerability of Three Formulations of CSL412 in Adults (≥ 18 to ≤ 45 Years) and Older Adults (≥ 60 Years)
Lead sponsor Seqirus, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Influenza
Intervention type Biological
Interventions CSL412, Inactivated trivalent influenza vaccine
Enrollment 612
Start date May 1, 2007
Primary completion Aug 1, 2007
Completion Aug 1, 2007
First posted May 28, 2007
Last update posted Jul 19, 2016
Countries United Kingdom

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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