BioMed Research International / 2013 / Article / Tab 2 / Review Article
Bilastine: A New Nonsedating Oral H1 Antihistamine for Treatment of Allergic Rhinoconjunctivitis and Urticaria Table 2 Randomized, double-blinded, parallel-group, placebo-controlled comparative studies of bilastine with other antihistamines: study characteristics and results of primary efficacy outcome measures.
Study Indication Primary outcome Arm 1;
Arm 2;
Arm 3;
Results for primary outcome [14 ] Seasonal allergic rhinitis AUC for TSS from baseline
14 days Bilastine 20 mg; 233 Desloratadine 5 mg; 242
Placebo; 245 Bilastine significantly better than placebo Bilastine versus desloratadine: NS [15 ] Seasonal allergic rhinitis AUC for TSS from baseline
14 days Bilastine 20 mg; 227 Cetirizine 10 mg; 228 Placebo; 226 Bilastine significantly better than placebo Bilastine versus cetirizine: NS [16 ] Perennial allergic rhinitis AUC for TSS from baseline
28 days Bilastine 20 mg; 214 Cetirizine 10 mg; 217 Placebo; 219 Bilastine versus cetirizine and placebo: NS [17 ] Chronic idiopathic urticaria Change in TSS from baseline
28 days Bilastine 20 mg; 173 Levocetirizine 5 mg; 165 Placebo; 184 Bilastine significantly better than placebo Bilastine versus levocetirizine: NS
AUC: area under curve; TSS: total symptom score; NS: not statistically significantly better.