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Completed Phase 2 Interventional Results available

A Trial of the Pharmacokinetics, Safety, and Tolerability of Subcutaneous Gamunex® in Primary Immunodeficiency

ClinicalTrials.gov ID: NCT00389324

Public ClinicalTrials.gov record NCT00389324. 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, 5:31 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

An Open-Label Single-Sequence, Crossover Trial to Evaluate the Pharmacokinetics and Safety of Subcutaneous Gamunex® 10% (Immune Globulin Intravenous [Human], 10% Caprylate/Chromatography Purified) in Subjects With Primary Immunodeficiency

Study identification

NCT ID
NCT00389324
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Grifols Therapeutics LLC
Industry
Enrollment
35 participants

Conditions and interventions

Interventions

  • Immune Globulin Intravenous (Human) Biological

Biological

Eligibility (public fields only)

Age range
13 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
Oct 31, 2006
Primary completion
Jul 31, 2008
Completion
Jul 31, 2008
Last update posted
Apr 19, 2015

2006 – 2008

United States locations

U.S. sites
6
U.S. states
5
U.S. cities
6
Facility City State ZIP Site status
University of California, Irvine Irvine California 92697
UCLA School of Medicine Los Angeles California 90095
Family Allergy & Asthma Center, PC Atlanta Georgia 30342
Allergy, Asthma & Immunology Associates, PC Omaha Nebraska 68124
Pediatric Allergy / Immunology Associates, PA Dallas Texas 75230
Virginia Commonwealth University Richmond Virginia 23219

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00389324, 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 Apr 19, 2015 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00389324 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →