Azelastine Nasal Spray Relieves Symptoms of Seasonal Allergic Rhinitis: Presented at AAAAI
Unregistered User
If this is not your name, click here.
Contact Us | Order Now | Journals | Bookstore | Register a colleague
 
  SEARCH  
News
Bookstore
Medline
The Web
Meetings & Congresses
Complete Doctor's Guide
 


 EXPLORE :
 news  All News
 webcasts All Webcasts
 All cases All Cases
 Meetings All Meetings & Congresses
 Medical All Medical Resources

top





New drugs / indications

English Dictionary

Medical Dictionary

Thesaurus



Warning | Privacy | Awards



 Favourite Journals 

Click here to choose your favourite journals


 Favourite Sites 

Click here to choose your favourite sites


 Languages 



  




Azelastine Nasal Spray Relieves Symptoms of Seasonal Allergic Rhinitis: Presented at AAAAI

By Maggie Schwarz

WASHINGTON, DC -- March 16, 2009 - Total seasonal allergic rhinitis score improves significantly over 14 days with azelastine 0.15% nasal spray, according to a study presented here at the American Academy of Allergy, Asthma & Immunology (AAAAI) Annual Meeting.

Julius Van Bavel, MD, Allergy and Asthma Associates, Austin, Texas, and colleagues evaluated a 0.15% azelastine hydrochloride solution, 2 sprays in each nostril once daily in 536 patients with moderate to severe seasonal allergic rhinitis during the 2007-2008 Texas Mountain Cedar season.

The investigators hypothesised that increasing the azelastine concentration from 0.1% to 0.15% would allow for once-daily dosing without increasing the incidence of adverse effects, Dr. Van Bavel said in a presentation on March 15.

The 0.15% formulation of azelastine is delivered in a sorbitol-based vehicle with sucralose as a taste-masking agent.

For their study, Dr. Van Bavel and colleagues randomised patients to azelastine or placebo once daily in the morning over a 14-day period and assessed the change from baseline in the 12-hour reflective Total Nasal Symptom Score (TNSS). The score consists of nasal congestion, sneezing, itchy nose, and runny nose.

After 2 weeks of treatment, mean improvement score and percentage improvement score were statistically significant with azelastine 0.15% compared with placebo (19% vs 10%, P < .001).

Mean improvement and percentage improvement scores were also statistically significant for azelastine 0.15% compared with placebo for instantaneous morning TNSS, which indicates efficacy with once-daily dosing (P < .001).

All individual symptoms of the TNSS were significantly improved with azelastine 0.15% compared with placebo (P < .01). With the exception of dysgeusia (4.5%) and nasal discomfort (4.5%), all other adverse events were reported at a similar incidence as placebo.

Dr. Van Bavel concluded that azelastine 0.15% was effective and well tolerated with once-daily dosing and might improve patients' compliance with nasal spray therapy.

Funding for this study was provided by Meda Pharmaceuticals.

[Presentation title: Efficacy and Safety of Azelastine (0.15%) Nasal Spray Administered Once Daily in Patients With Seasonal Allergic Rhinitis. Abstract 492]

E-mail this page
to a friend or colleague!
To print,
use this version




Any question regarding a medical diagnosis, treatment, referral, drug availability or pricing should be directed to either a licensed physician or to the product's manufacturer.

If you have any technical questions or other concerns about this site, feel free to contact us at webmaster@docguide.com.

All contents Copyright (c) 1995- Doctor's Guide Publishing Limited. All rights reserved.


Employment opportunities | Partnering opportunities