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Completed Phase 3 Interventional Results available

Safety Study of Levocetirizine Dihydrochloride Oral Liquid Formulation in Children Aged 1 to Less Than 6 Years Suffering From Allergic Rhinitis or Chronic Urticaria of Unknown Origin

ClinicalTrials.gov ID: NCT00619801

Public ClinicalTrials.gov record NCT00619801. 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 Sep 1, 2026, 10:20 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

A Multi-Center, Randomized, Double Blind, Placebo Controlled Parallel Group Study of the Safety of Levocetirizine Dihydrochloride Oral Liquid Formulation b.i.d Dosing in Children Aged 1 to < 6 Years Suffering From Allergic Rhinitis or Chronic Urticaria of Unknown Origin

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine the safety of the oral formulation of levocetirizine in children ages 1 to less than 6 years old who suffer from allergic rhinitis or chronic urticaria of unknown origin.

Study identification

NCT ID
NCT00619801
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Pharma
Industry
Enrollment
173 participants

Conditions and interventions

Eligibility (public fields only)

Age range
2 Years to 6 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 29, 2008
Primary completion
Jun 30, 2008
Completion
Jun 30, 2008
Last update posted
Mar 5, 2015

2008

United States locations

U.S. sites
28
U.S. states
16
U.S. cities
28
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Little Rock Arkansas
Not listed Beverly Hills California
Not listed Crescent City California
Not listed Huntington Beach California
Not listed Mission Viejo California
Not listed San Diego California
Not listed Wildomar California
Not listed Denver Colorado
Not listed Pueblo Colorado
Not listed Savannah Georgia
Not listed Stockbridge Georgia
Not listed Normal Illinois
Not listed Overlook Park Kansas
Not listed Owensboro Kentucky
Not listed Metarie Louisiana
Not listed Baltimore Maryland
Not listed Omaha Nebraska
Not listed Papillon Nebraska
Not listed Oklahoma City Oklahoma
Not listed Medford Oregon
Not listed Portland Oregon
Not listed Barnwell South Carolina
Not listed Charleston South Carolina
Not listed Dallas Texas
Not listed El Paso Texas
Not listed New Braunfels Texas
Not listed Richmond Virginia

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 NCT00619801, 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 Mar 5, 2015 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00619801 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →