Clinical trial

Safety and Efficacy of Intravenous Immunoglobulin IgPro10 in Patients With…

NCT00322556 · CSL Behring, Industry · Completed

Key facts

NCT number NCT00322556
Title Safety and Efficacy of Intravenous Immunoglobulin IgPro10 in Patients With Primary Immunodeficiencies (PID)
Official title A Multicenter Extension Study on the Safety and Efficacy of IgPro10 in Patients With Primary Immunodeficiency (PID)
Lead sponsor CSL Behring, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Agammaglobulinemia, IgG Deficiency, Common Variable Immunodeficiency
Intervention type Drug
Interventions Immunoglobulins Intravenous (Human)
Enrollment 55
Start date Nov 1, 2005
Primary completion Apr 1, 2008
Completion Apr 1, 2008
First posted May 8, 2006
Last update posted Oct 26, 2012
Countries United States

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

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

Browse all ClinicalTrials.gov studies