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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 Jul 23, 2026, 12:00 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.

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

Interventions

  • Levocetirizine 1.25 mg Drug
  • Placebo Other

Drug · Other

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
Feb 29, 2008
Primary completion
Aug 31, 2008
Completion
Aug 31, 2008
Last update posted
Mar 5, 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 5, 2015 · Synced Jul 23, 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 NCT00628108 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →