News
Drug Development
FDA
Manufacturing
Deals
Business
Job Trends
Cell and Gene Therapy
Cancer
Opinions
Press Releases
All News & Releases
Podcasts
Events
Jobs
Companies
Hotbeds
More
Reports
Career Advice
NextGen: Top Startups to Watch
40 Under 40
Best Places to Work
Employer Resources
Advertise
Advertise
Talent Solutions
Post Jobs
Submit a Press Release
Submit an Event
SUBSCRIBE
Menu
SUBSCRIBE
Show Search
News
Drug Development
FDA
Manufacturing
Deals
Business
Job Trends
Cell and Gene Therapy
Cancer
Opinions
Press Releases
All News & Releases
Podcasts
Events
Jobs
Companies
Hotbeds
More
Reports
Career Advice
NextGen: Top Startups to Watch
40 Under 40
Best Places to Work
Employer Resources
Advertise
Advertise
Talent Solutions
Post Jobs
Submit a Press Release
Submit an Event
Search Query
Submit Search
News
FDA
Bristol-Myers Squibb Company: ONGLYZATM (saxagliptin) Receives Marketing Authorisation In Europe For The Treatment Of Type 2 Diabetes
October 5, 2009
|
1 min read
Twitter
LinkedIn
Facebook
Email
Print
PARIS & LONDON--(BUSINESS WIRE)--Bristol-Myers Squibb Company (NYSE: BMY) and AstraZeneca (NYSE/LSE: AZN) announced today that the European Commission has granted marketing authorisation for ONGLYZATM in the 27 countries of the European Union.
Twitter
LinkedIn
Facebook
Email
Print
FDA
Approvals
Europe
Bristol Myers Squibb Company
MORE ON THIS TOPIC
Opinion
The next FDA commissioner must be a champion for gene therapies
June 5, 2026
·
4 min read
·
Erik Paulsen
Regulatory
Stakeholders want Makary’s voucher program paused, call for FDA independence
June 5, 2026
·
3 min read
·
Tristan Manalac
Manufacturing
FDA hits Medline with warning letter over long-running contamination problem
June 3, 2026
·
2 min read
·
Nick Paul Taylor
Policy
FDA taps prior knowledge to expedite cell and gene therapy development
June 3, 2026
·
12 min read
·
BioSpace Editorial Staff