Clinical Trials Directory

Trials / Completed

CompletedNCT00780403

Multi-Center, Pediatric, Open-Label, Preference Study of Desloratadine 2.5 mg Reditab (SCH34117) and Zyrtec ® 5.0 mg Chewable Tablet Medications (Study P04573) (Completed)

A Multi-Center, Pediatric, Open-Label, Preference Study of Desloratadine 2.5 mg Reditab (SCH34117) and Zyrtec ® 5.0 mg Chewable Tablet Medications

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
220 (actual)
Sponsor
Organon and Co · Industry
Sex
All
Age
6 Years – 11 Years
Healthy volunteers
Accepted

Summary

The primary objective of this study was to determine whether children ages 6-11 years prefer desloratadine RediTabs (2.5 mg) or a marketed competitor (Zyrtec® 5 mg Chewable Tablets). The secondary objectives of this study were to compare acceptance of the two attributes, taste and feeling in the mouth, of desloratadine 2.5 mg RediTabs and Zyrtec® 5 mg Chewable Tablets

Conditions

Interventions

TypeNameDescription
DRUGDesloratadinedesloratadine RediTabs, 1 tablet (2.5 mg),oral administration, single day
DRUGZyrtec® (cetirizine)Zyrtec® (cetirizine) Chewable Tablets, 1 tablet (5 mg), oral administration, single day

Timeline

Start date
2005-08-01
Primary completion
2005-10-01
Completion
2005-10-01
First posted
2008-10-27
Last updated
2022-02-09
Results posted
2010-07-30

Source: ClinicalTrials.gov record NCT00780403. Inclusion in this directory is not an endorsement.