Free Newsletter
Wyeth seeking regulatory approval for Prevnar-13
Wyeth is putting the finishing touches on its regulatory application for Prevnar-13, the latest generation in a series of jabs that defend against pneumococcal disease. Wyeth researchers say that this version could offer broader protection against the bacteria that triggers pneumococcal disease and extend its effectiveness to older adults. The applications will be filed in the U.S. and Europe early next year.
"We haven't gotten rid of all the diseases," said Matt Moore, medical epidemiologist with the CDC. "That's our goal. We want to get rid of it all."
The blockbuster Prevnar was originally introduced in 2000, when streptococcus pneumonia caused 21 to 33 cases per 100,000 population each year. That number has now dropped to 13. Late stage data on Prevnar-13 will be released later this month. Wyeth does face new competition, though, from GlaxoSmithKline.
- read the report from the Wall Street Journal
Related Articles:
Whistleblowers allege problems with Wyeth's Prevnar
Pharma execs practice positive thinking
Pneumococcal rates down sharply post-vaccine
Comments
Post new comment
Paid Research Reports
- The Specialty Pharma Market Outlook: Key players, new company growth models and emerging opportunities
- Investigating Clinical Trial Costs: Comparative analysis of trial cost components in key geographies
- Clinical Trial Recruitment Strategies: Optimizing patient recruitment and retention in late stage clinical trials
- Pipeline Insight: Therapeutic Cancer Vaccines - Prospect of first approval set to reinvigorate interest from major companies
- Stakeholder Opinions: Vaccines in Emerging Markets (Asia) - Opportunities in China, India, South Korea and Taiwan
- Big Pharma Performance Before, During and Beyond the Global Recession




