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
| Type | Name | Description |
|---|---|---|
| DRUG | Desloratadine | desloratadine RediTabs, 1 tablet (2.5 mg),oral administration, single day |
| DRUG | Zyrtec® (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.