A Study of Plasma-Derived Human Butyrylcholinesterase Administered Intramuscularly

This study has been completed.
Sponsor:
Collaborator:
DynPort Vaccine Company LLC, A CSC Company
Information provided by (Responsible Party):
Baxalta US Inc.
ClinicalTrials.gov Identifier:
NCT00333528
First received: June 1, 2006
Last updated: June 26, 2015
Last verified: January 2009
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study has been completed.
  Study Completion Date: August 2008
  Primary Completion Date: April 2008 (Final data collection date for primary outcome measure)