Trials / Completed
CompletedNCT02182544
WAL801CL (Epinastine Hydrochloride) Dry Syrup in Paediatric Perennial Allergic Rhinitis
Phase III Double-blind Comparative Study of WAL801CL Dry Syrup in Paediatric Perennial Allergic Rhinitis
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 151 (actual)
- Sponsor
- Boehringer Ingelheim · Industry
- Sex
- All
- Age
- 15 Years
- Healthy volunteers
- Not accepted
Summary
Study to investigate the efficacy of WAL801CL Dry Syrup in comparison with ketotifen fumarate on pediatric perennial allergic rhinitis and to evaluate the safety of WAL801CL Dry Syrup compared to ketotifen fumarate and to confirm the appropriateness of dosage of WAL801 Dry Syrup.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | WAL801CL dry syrup | |
| DRUG | Ketotifen fumarate dry syrup | |
| DRUG | Ketotifen fumarate dry syrup placebo | |
| DRUG | WAL 801 CL dry syrup placebo |
Timeline
- Start date
- 2001-06-01
- Primary completion
- 2001-12-01
- First posted
- 2014-07-08
- Last updated
- 2014-07-14
Source: ClinicalTrials.gov record NCT02182544. Inclusion in this directory is not an endorsement.