CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 25 enrolled
Drug / intervention
ACAM2000biological
Likely dose
ACAM2000 2.5µgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01158157
NCT01158157Phase 3Completed

Vaccinia Vaccine (ACAM2000) for the Production of Vaccinia Immune Globulin Intravenous (VIGIV)

Emergent BioSolutions·interventional·Posted Jul 8, 2010·Updated Mar 18, 2024

In Brief

A Phase 3 clinical trial evaluating ACAM2000 for Smallpox Vaccine Adverse Reaction. Completed, enrolled 25 participants across 1 site.

Detailed Summary

The purpose of this study is to vaccinate plasma donors with ACAM2000 smallpox vaccine for collection of plasma to be used in the manufacturing of Vaccinia Immune Globulin Intravenous (VIGIV).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 3CompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedJul 8, 2010
Enrollment StartSep 13, 2010
Primary CompletionFeb 14, 2012
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 16.0 years ago

Interventions

ACAM2000biological

Percutaneous administration of a droplet (2.5µg) of ACAM2000 using a bifurcated needle.