The European Commission (EC) published the 8th Report on Monitoring Patent Settlements. It covers the 107 pharmaceutical patent settlements concluded between originator and generic drug companies in 2016 and shows that pay-for-delay settlements continue to decline. Such settlements can contravene antitrust laws with originator manufactures paying-off generics companies to delay generics market entry. Pay-offs can be monetary, but may also include distribution or licensing agreements or restrictions.
EU report finds decline in pay-for-delay pharma deals
Home/Reports | Posted 27/04/2018 0 Post your comment
The creation of the eight reports on patent settlements result from a Commission led inquiry into competition within the pharmaceutical sector which concluded in 2009. In follow-up to this, they began their annual monitoring of pharmaceutical companies to assess how they impact the market entry of generics [1-4].
The 8th report shows that, in 2016, only 11% of deals limited generics market entry and involved value transfer from the originator to the generics manufacturer. From 2004 to 2008, such deals represented 22% of all settlements. The Commission also noted that over 90% of the deals made in 2016 do not require competition law scrutiny.
Of the 2016 settlements, the Commission categorized 27% as being without limitation to generics market entry. A further 62% were said to limit generics market entry, but without a transfer of value from the originator to the generics company. Most of the latter settlements were signed in the context Portuguese legislation that came into force in 2011. This has led to increased arbitration proceedings between originator product sponsors and generics companies applying for marketing authorization.
The EC’s results show that their monitoring exercises and scrutinization of value transfer settlements in the pharmaceutical industry has not prevented companies from settling patent disputes. It also states that the number of generics entry-limiting settlements that involve a transfer of value have now ‘stabilized at a low level’.
Related articles
GSK fined GBP 37.6 million in pay-for-delay appeal
Pay-for-delay bill reintroduced
References
1. GaBI Online - Generics and Biosimilars Initiative. Problematic pharma patent settlements decrease in the EU [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2018 Apr 27]. Available from: www.gabionline.net/Reports/Problematic-pharma-patent-settlements-decrease-in-the-EU
2. GaBI Online - Generics and Biosimilars Initiative. EU problematic patent settlements remain at low level [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2018 Apr 27]. Available from: www.gabionline.net/Reports/EU-problematic-patent-settlements-remain-at-low-level
3. GaBI Online - Generics and Biosimilars Initiative. EU problematic patent settlements stabilize [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2018 Apr 27]. Available from: www.gabionline.net/Reports/EU-problematic-patent-settlements-stabilize
4. GaBI Online - Generics and Biosimilars Initiative. EU investigation tackles pay for delay [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2018 Apr 27]. Available from: www.gabionline.net/Reports/EU-investigation-tackles-pay-for-delay
Permission granted to reproduce for personal and non-commercial use only. All other reproduction, copy or reprinting of all or part of any ‘Content’ found on this website is strictly prohibited without the prior consent of the publisher. Contact the publisher to obtain permission before redistributing.
Copyright – Unless otherwise stated all contents of this website are © 2018 Pro Pharma Communications International. All Rights Reserved.
Guidelines
Regulatory update for post-registration of biological products in Brazil
New regulations in Brazil for the registration of biosimilars
Policies & Legislation
NPRA Malaysia trials new timelines for variation applications
Regulatory evolution and impact of simplified requirements for interchangeable biosimilars in the US
Comments (0)
Post your comment