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Completed Phase 3 Interventional Results available

Safety Study of Levocetirizine Dihydrochloride Oral Liquid Formulation in Children Aged 6 Months to 11 Months

ClinicalTrials.gov ID: NCT00628108

Public ClinicalTrials.gov record NCT00628108. 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 Oct 22, 2026, 5:36 AM 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 in Children Aged 6 Months to 11 Months With Symptoms of Allergic Rhinitis or Chronic Urticaria.

Brief summary

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

To determine the safety of levocetirizine in children ages 6-11 months with symptoms of allergic rhinitis or chronic idiopathic urticaria.

Study identification

NCT ID
NCT00628108
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Pharma
Industry
Enrollment
69 participants

Conditions and interventions

Eligibility (public fields only)

Age range
6 Months to 11 Months
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
Mar 2008 (Type not available)
Primary completion
Sep 2008 (Actual)
Completion
Sep 2008 (Actual)
Last update posted
Mar 6, 2015

2008

United States locations

U.S. sites
26
U.S. states
12
U.S. cities
26
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Hot Springs Arkansas — —
Not listed Jonesboro Arkansas — —
Not listed Little Rock Arkansas — —
Not listed Bakersfield California — —
Not listed Crescent City California — —
Not listed Huntington Beach California — —
Not listed Los Angeles California — —
Not listed Orange California — —
Not listed Roseville California — —
Not listed Stockton California — —
Not listed Albany Georgia — —
Not listed Gainesville Georgia — —
Not listed Normal Illinois — —
Not listed Bridgeton Missouri — —
Not listed Omaha Nebraska — —
Not listed Oklahoma City Oklahoma — —
Not listed Barnwell South Carolina — —
Not listed Spartanburg South Carolina — —
Not listed Kingsport Tennessee — —
Not listed Austin Texas — —
Not listed Dallas Texas — —
Not listed El Paso Texas — —
Not listed San Antonio Texas — —
Not listed Sugarland 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 NCT00628108, 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 6, 2015 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00628108 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →