drugset / Trial / NCT01108783
A Phase III Efficacy Study of the Symptomatic Treatment of Seasonal Allergic Rhinitis With Bilastine
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The objective of the study was to determine the efficacy and tolerability of 20 mg of Bilastine, compared to Desloratadine and placebo for the treatment of Seasonal Allergic Rhinitis.
Timeline
- Start
- 2003-04
- Primary completion
- 2003-08
- Completion
- 2004-02
Outcome
Met primary endpoint
paper significantly reduced the AUC of TSS to a greater degree from baseline compared to placebo (98.4 with bilastine vs 118.4 with placebo; P < 0.001) PMID 19132976 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bilastine | Small molecule | 20 mg | — |
| Comparator | Desloratadine | Small molecule | 5 mg | — |