Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed No phase listed Observational

Octagam 5% Versus Comparator Post Marketing Trial

ClinicalTrials.gov ID: NCT01859754

Public ClinicalTrials.gov record NCT01859754. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 10:13 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Postmarketing Requirement Non-Interventional 2-armed Study to Evaluate the Safety of Octagam® Immune Globulin Intravenous (Human) 5% Liquid Preparation, With a Special Emphasis on Monitoring, Analysis and Reporting of Thromboembolic Events

Study identification

NCT ID
NCT01859754
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Octapharma
Industry
Enrollment
623 participants

Conditions and interventions

Interventions

  • Octagam 5% Biological
  • Other marketed IVIG product Biological

Biological

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 20, 2013
Primary completion
May 21, 2019
Completion
May 21, 2019
Last update posted
Jun 9, 2019

2013 – 2019

United States locations

U.S. sites
27
U.S. states
16
U.S. cities
25
Facility City State ZIP Site status
Octapharma Research Site Granada Hills California 91344
Octapharma Research Site Irvine California 92697
Octapharma Research Site Los Angeles California 90025
Octapharma Research Site Redlands California 92373
Octapharma Research Site Centennial Colorado 80112
Octapharma Research Site Roswell Georgia 30076
Octapharma Research Site Chicago Illinois 60612
Octapharma Research Site Springfield Illinois 62701
Octapharma Research Site Fort Wayne Indiana 46815
Octapharma Research Site Wichita Kansas 67201
Octapharma Research Site Fort Mitchell Kentucky 41017
Octapharma Research Site Farmington Hills Michigan 48334
Octapharma Research Site Plymouth Minnesota 55446
Octapharma Research Site Plymouth Minnesota 55447
Octapharma Research Site Omaha Nebraska 68124
Octapharma Research Site East Setauket New York 11733
Octapharma Research Site New York New York 10012
Octapharma Research Site New York New York 10065
Octapharma Research Site Columbus Ohio 43235
Octapharma Research Site Mayfield Heights Ohio 44124
Octapharma Research Site Toledo Ohio 43617
Octapharma Research Site Pawtucket Rhode Island 02860
Octapharma Research Site Anderson South Carolina 29621
Octapharma Research Site Nashville Tennessee 37203
Octapharma Research Site Amarillo Texas 79124
Octapharma Research Site Dallas Texas 75231
Octapharma Research Site Irving Texas 75014

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01859754, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 9, 2019 · Synced Jul 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01859754 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →