Efficacy and Safety of Azelastine Hydrocloride and Fluticasone Propionate Combined in a Single Nasal Spray Delivery Device in Patients with Seasonal Allergic Rhinitis

2009 ◽  
Vol 123 (2) ◽  
pp. S155-S155 ◽  
Author(s):  
F. Hampel ◽  
P. Ratner ◽  
J. Diaz ◽  
H. Sacks
2018 ◽  
Vol 141 (2) ◽  
pp. AB173 ◽  
Author(s):  
Frank C. Hampel ◽  
Andrew J. Pedinoff ◽  
Robert L. Jacobs ◽  
Aurora Breazna ◽  
Cynthia F. Caracta ◽  
...  

Allergy ◽  
1995 ◽  
Vol 50 (6) ◽  
pp. 498-505 ◽  
Author(s):  
A. Boner ◽  
L Sette ◽  
L. Martinati ◽  
R. K. Sharma ◽  
D. H. Richards

1997 ◽  
Vol 11 (4) ◽  
pp. 323-330 ◽  
Author(s):  
Martin A. Stern ◽  
Ronald Dahl ◽  
Lars P. Nielsen ◽  
Bente Pedersen ◽  
Camilla Schrewelius

The efficacy of aqueous suspensions of budesonide nasal spray and fluticasone propionate nasal spray, in the treatment of seasonal allergic rhinitis, was compared in a large, placebo-controlled, two-center study. A 1-week baseline period was followed by a 4- to 6-week treatment period during which 635 adult patients, aged 18–72 years, were randomized to receive either placebo, budesonide 128 μg, or 256 μg once daily, or fluticasone propionate, 200 μg once daily. Nasal and eye symptoms, overall treatment efficacy and safety assessments were made during the study period. Combined, as well as individual, nasal symptoms were significantly improved in all three active treatment groups compared with placebo therapy. Treatment with 256 μg/day of budesonide was found to be significantly more effective in reducing the sneezing score compared with 200 μg/day of fluticasone propionate. Analysis of symptom scores on days when the pollen count was greater than 10 grains/m3 revealed 256 μg/day of budesonide therapy to be significantly more effective in reducing combined symptom scores as well as the individual scores for sneezing and runny nose, compared with 200 μg/day fluticasone propionate. The higher dose of budesonide (256 μg/day) was also more effective than the lower dose (128 μg/day) in reducing sneezing scores and statistical significance was almost reached for the reduction in combined symptom and runny nose scores. Substantial or total control of symptoms was achieved by 31.4%, 85.3%, 88.4%, and 81.9% of patients receiving placebo, 128 μg/day of budesonide, 256 μg/day of budesonide, and 200 μg/day of fluticasone propionate, respectively. The incidence of adverse events was low in all treatment groups. In conclusion, both budesonide and fluticasone propionate treatments were effective and well-tolerated in the treatment of seasonal allergic rhinitis. However, 256 μg/day of budesonide tended to be more effective than 200 μg/day of fluticasone propionate and 128 μg/day of budesonide, especially when patients were exposed to a higher pollen load.


2019 ◽  
Vol 122 (6) ◽  
pp. 630-638.e3 ◽  
Author(s):  
Gary N. Gross ◽  
Gary Berman ◽  
Niran J. Amar ◽  
Cynthia F. Caracta ◽  
Sudeesh K. Tantry

2003 ◽  
Vol 91 (1) ◽  
pp. 44-48 ◽  
Author(s):  
Mark S. Dykewicz ◽  
Harold B. Kaiser ◽  
Robert A. Nathan ◽  
Stacey Goode-Sellers ◽  
Cindy K. Cook ◽  
...  

2006 ◽  
Vol 96 (6) ◽  
pp. 851-857 ◽  
Author(s):  
Bruce G. Martin ◽  
Charles P. Andrews ◽  
Julius H. van Bavel ◽  
Frank C. Hampel ◽  
Kristofer C. Klein ◽  
...  

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