Antibiotic Resistance Program Launched in Europe - Pharmaceutical Technology

Latest Issue
PharmTech

Latest Issue
PharmTech Europe

Antibiotic Resistance Program Launched in Europe



The European Federation of Pharmaceutical Industries and Associations (EFPIA) has welcomed the launch of a €223.7-million ($276.5 million) program to tackle antimicrobial resistance and speed up the development of new antibiotics. The program was launched by the Innovative Medicines Initiative (IMI), a public–private partnership, and builds on the European Commission’s Action Plan against the rising threats from Antimicrobial Resistance, which was launched in November 2011.

The program will bring together leading academics and five major pharmaceutical companies. The IMI has issued a call for proposals and has set aside a budget of up to €223.7 million ($276.5 million) in funding, with €109 million ($134.8 million) coming from the IMI and a further €114.7 million ($141.8 million) coming from contributions by participating EFPIA companies.

Michael Goldman, executive director of the IMI, said in a statement, “This is a historic opportunity for Europe to overcome a public health problem which threatens millions of lives worldwide. For researchers in universities, hospitals and small and medium-sized enterprises it is also a unique opportunity to speed up their research in the area of antimicrobial resistance, as the collaboration will give them access to the knowledge and expertise of the pharmaceutical industry.”

According to the IMI, antibacterial drug development is no longer a financially viable option for pharmaceutical companies. As well as scientific challenges and complex regulatory requirements, the cost of developing an antibiotic outweighs the potential returns on investment.

The IMI’s program is expected to use approximately €600 million in funding over the next seven years. Initial projects will focus on building and training networksof researchers, facilitating and increasing the exchange of research data, and improving the efficiency of clinical trials.

Richard Bergström, director-general of EFPIA said, “Our researchers and the scientific community have realized that we can only deal with this urgent threat by working together and pooling our knowledge.... by co-funding clinical trials, policy makers in Europe have created a strong incentive for companies and investors to come back to this field of research.”

ADVERTISEMENT

blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
|Monthly
| Weekly

Survey
How does your company apply quality-by-design (QbD) principles to manufacturing processes?
To all processes for both new and legacy products
To all process for new products only
To select process for new products only
To select processes for both new and legacy products
Do not use QbD
To all processes for both new and legacy products
20%
To all process for new products only
13%
To select process for new products only
25%
To select processes for both new and legacy products
20%
Do not use QbD
23%
View Results
UPCOMING CONFERENCES

Programs for Investigational and Pre-Launch Drugs
Philadelphia, PA
July 17-18, 2013
Request Brochure

Strategic Pipeline Planning & Portfolio Valuation
Philadelphia, PA
August 13-14, 2013
Request Brochure

MES 2013 - Forum on Manufacturing Execution Systems
Philadelphia, PA
August 14-15, 2013
Request Brochure

Mobile Innovation for the Life Sciences Industry
Philadelphia, PA
August 20-21, 2013
Request Brochure

See All Conferences >>

Eric Langer Outsourcing Outlook Eric LangerOutsourcing's Modest Role as a Cost-Containment Strategy
Patricia Van Arnum Ingredients Insider Patricia Van ArnumIntellectual Property Battles in Solid-State Chemistry
Nathan Jessop Industry Insider Nathan Jessop Campaign Against Counterfeit Drugs Continues
Lynn Torbeck Statistical Solutions Lynn D. TorbeckCompositing Samples and the Risk to Product Quality
 More
Global Biosimilars Market to Reach $2.445 Billion in 2013
Adapting to Change
AstraZeneca and Exco InTouch Collaborate to Augment Current COPD Pathways
Overcoming the Challenges in Biopharmaceutical Stability Testing
PhRMA Dismayed by Special 301 Report
FindPharma Custom Search

Click here