spacer
home > epc > winter 2002 > prescription drug co-promotion: 21st century dealmaking
PUBLICATIONS
European Pharmaceutical Contractor

Prescription Drug Co-Promotion: 21st Century Dealmaking

The pharmaceutical industry has experienced a flurry of announced and, to a lesser extent, consummated mergers in the US and Western Europe in the past decade. Many of these business combinations appear to have been driven by a desire to access promising drug pipelines, consolidate research and development efforts, penetrate specific geographic markets for prescription drugs (often the US where foreign partners are involved) and rationalise regulatory and sales functions.

Often overlooked in this flurry of M&A activity however, is the growing trend among pharmaceutical companies, large and small, to achieve many of the benefits of 'traditional' business combinations by engaging in 'blockbuster' drug co-promotion activity where two life science companies collaborate in the marketing of very promising prescription drugs. In some of the recent, more complex co-promotions, co-operating companies pool their resources and strengths in conducting clinical trials, obtaining requisite regulatory and, for example in Western Europe, pricing, approvals and mass marketing and detailing the product.

For pharmaceutical companies, these types of co-promotion can result in significant revenue enhancement without the issues of post-deal integration and cost synergy management following strategic mergers. A number of pharmaceutical companies have supplemented strategic mergers with these types of co-promotions. For other companies who are developing potentially promising blockbuster drugs, co-promotion can offer upfront and milestone cash infusions, access to complimentary technology and, with the appropriate marketing partner, increased prospects for a successful drug launch.


Read full article from PDF >>

Rate this article You must be a member of the site to make a vote.  
Average rating:
0
     

There are no comments in regards to this article.

Banner of CRS on Samedan
spacer
By David Schulman, David Wallis and Helen Hunsperger at International Law Firm Dechert

The authors have extensive experience both in the US and in Europe, advising a variety of life science companies.

David Schulman is a Partner and US-qualified lawyer working in Dechert's London office, resident since 1999. His work on behalf of these clients includes advising on co-promotions, licenses and distribution arrangements for life sciences and other technology-based companies.


David graduated from the University of Pennsylvania with a BA in 1982 and a JD in 1985 and attended the University of Edinburgh as part of a general course study in 1981.

David Wallis is a Partner in Dechert's London office. He qualified as a solicitor in 1989. David graduated from Oxford Brookes University in 1985 with a First Class Degree in Law and English, and from Guildford College of Law in 1986. Helen Hunsperger is a Assistant Solicitor in Dechert's London office. Helen trained with Dechert and qualified in 1999 after graduating from Nottingham Trent University in 1991 with an LLB Honours Degree.


spacer
David Wallis
spacer
spacer
spacer
David Schulman
spacer
spacer
spacer
Helen Hunsperger
spacer
spacer
Print this page
Send to a friend
Privacy statement

Industry Events

10th-Anniversary Event RFID Journal LIVE! 2012

3-5 April 2012, Walt Disney World Swan and Dolphin Resort, Orlando, Florida

RFID Journal LIVE! 2012, our tenth annual conference and exhibition, is the only event where you can learn how to use RFID technologies to improve your pharmaceutical and medical packaging business, from real-world case studies across all applications, including asset tracking, logistics and transportation, supply chain management, warehouse and inventory management, security and more. Learn from a customized program featuring more than 50 end-user case studies and 8 industry-specific and how-to conference tracks.  
More info >>

 
News and Press Releases

Norwich Expands Capabilities for Phase I-III Clinical Trials

Norwich Clinical Services (NCS), a global provider of clinical research services for the pharmaceutical and biotech industries, today announced a significant expansion to its clinical research capabilities in order to meet growing market demand. Primary to the expansion, NCS unveiled a new clinical facility with capabilities to conduct all aspects of Phase I – III clinical trials including pharmacokinetics in healthy volunteers, bio-availability and bio-equivalence studies, drug metabolism studies, dose proportionality studies and multiple dose studies.
More info >>

 

 

Buy Atrovent Online no prescription Buy Symbicort Online no prescription Buy Flovent Online no prescription Buy Flonase Online no prescription Buy Rhinocort Online no prescription Buy Allegra Online no prescription Buy Advair Online no prescription Buy Combivent Online no prescription Buy Astelin Online no prescription Buy Spiriva Online no prescription Buy Ventolin Online no prescription
©2000-2011 Samedan Ltd.
Add to favourites

Print this page

Send to a friend
Privacy statement
.