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NCT00619801 · ClinicalTrials.gov registry record · Phase 3

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

A Phase 3 study, sponsored by UCB Pharma.

Completed
Registry status
Phase 3
Development phase
173
Enrollment target

NCT00619801: Completed Phase 3 study, sponsored by UCB Pharma.

NCT00619801 is a Phase 3 study that has completed, run by UCB Pharma. The registered enrollment target is 173 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (78% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00619801, a Phase 3 study, has completed, sponsored by UCB Pharma.

COMPLETED
Registry status
Phase 3
Development phase
173 participants
Enrollment target

Study Summary

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.

Interventions

  • DRUG Placebo
  • DRUG Levocetirizine

Trial Details

FieldValue
Enrollment Target 173 participants
Start Date 2008-03
Est. Completion 2008-07
Phase Phase 3
UCB Pharma

100 total trials

What the finished NCT00619801 record still lists

NCT00619801 is an interventional study that assigns participants to a tested intervention. The registered 173 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (78% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00619801 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00619801 about?

NCT00619801 is a clinical study titled "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". 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.

What is the current status of trial NCT00619801?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 173 participants. The study started on 2008-03. Estimated completion is 2008-07.

What interventions are being tested in trial NCT00619801?

The interventions under investigation include: Placebo (DRUG), Levocetirizine (DRUG).

Who is sponsoring clinical trial NCT00619801?

This trial is sponsored by UCB Pharma, which has 100 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00619801's enrollment target sits among peer trials

173 1445th of 2000 higher than 553 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00619801, the US trial registry maintained by the National Library of Medicine. NCT00619801 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.