China Biopharmaceuticals Holdings has announced the completion of all required clinical trials for desloratadine tablets for seasonal allergic rhinitis. The studies were conducted in six hospitals throughout China. The results have been sent to the Chinese State Food and Drug Administration (SFDA) for manufacturing and marketing approval. The company anticipates an approval response from the agency in the second half of 2007.
Desloratadine is indicated for the relief of the nasal and non-nasal symptoms of seasonal allergic rhinitis, as well as the symptomatic relief of pruritus and the reduction in the number of hives, and size of hives, in patients with chronic idiopathic urticaria.
In China, 30% of the population has suffered from an allergy at least once. The $1.5 billion allergy drug market in the country continues to grow at a rate of 15% per year, according to the company.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze