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Completed Phase 3 Interventional Results available

Study of Octanorm Subcutaneous IG in Patients With PID

ClinicalTrials.gov ID: NCT01888484

Public ClinicalTrials.gov record NCT01888484. 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 22, 2026, 12:04 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

Clinical Phase III Study to Evaluate the Pharmacokinetics, Efficacy, Tolerability and Safety of Subcutaneous Human Immunoglobulin (Octanorm 16.5%) In Patients With Primary Immunodeficiency Diseases

Study identification

NCT ID
NCT01888484
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Octapharma
Industry
Enrollment
75 participants

Conditions and interventions

Interventions

  • octanorm 16.5% Biological

Biological

Eligibility (public fields only)

Age range
2 Years to 75 Years
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
Feb 28, 2014
Primary completion
Jun 8, 2020
Completion
Jun 8, 2020
Last update posted
Aug 16, 2021

2014 – 2020

United States locations

U.S. sites
7
U.S. states
6
U.S. cities
7
Facility City State ZIP Site status
Octapharma Research Site Birmingham Alabama 35233
Octapharma Research Site Irvine California 92697
Octapharma Research Site San Diego California 92123
Octapharma Research Site Centennial Colorado 80112
Octapharma Research Site Omaha Nebraska 68046
Octapharma Research Site Toledo Ohio 43617
Octapharma Research Site Frisco Texas 75034

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01888484, 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 Aug 16, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01888484 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →