US President Barack Obama’s plan for economic growth and deficit reduction, announced on 19 September 2011, recommends a series of healthcare reforms. The proposals include higher drug rebates for low-income patients, banning pay-to-delay deals between generics and originator companies and reducing biologicals exclusivity from 12 to seven years. The proposals aim to save US$320 billion in healthcare spending over 10 years.
Generics and biosimilars affected by Obama’s deficit plans
Biosimilars/News
|
Posted 23/09/2011
0
Post your comment
![picture55 picture55](/var/gabi/storage/images/media/images/picture55/6155-3-eng-GB/picture55_large.jpg)
Drugmaker cuts
Brand-name drugmakers would be asked to give a 23% discount or rebate to the government for low-income patients who get a subsidy to pay for drugs. Generic drugmakers would have to give a 13% rebate. The drug rebates are expected to save the government US$135 billion over 10 years.
This is not good news for generics manufacturers who may already be operating on low margins in the highly competitive US generics market.
Banning pay-to-delay deals
President Obama is also proposing a ban on the somewhat controversial pay-to-delay deals.
The Federal Trade Commission (FTC) has for years opposed pay-to-delay patent litigation settlements, in which a brand-name drug manufacturer compensates its generics competitor to delay entering the market and offering patients a lower-cost alternative.
According to the FTC these deals delay the introduction of lower-cost medicines by an average of 17 months [1] and cost consumers and taxpayers US$3.5 billion a year in higher drug prices.
The Generic Pharmaceutical Association (GPhA), however, has reacted with concern over the proposal to ban patent settlements. The GPhA disagrees that these deals delay generic entry arguing that ‘patent settlements have never prevented competition beyond a patent’s expiration, and in many cases have resulted in making lower-cost generics available months and even years before patents have expired. In fact, of the 23 new generic drug launches expected in 2011, settlements made 17 of these possible where the generic will launch prior to a patent’s expiration’ [1].
Biologicals exclusivity
The plan intends to reduce biologicals market exclusivity from the 12 years foreseen in the BPCI Act to seven years, as previously proposed by President Obama in his 2012 budget proposal.
This, if it goes ahead, would be great news for biosimilar products which could be launched five years earlier.
Related articles
More debate over ‘pay-to-delay’ legislation in the US
Battle over ‘pay-for-delay’ deals continues
US bill to curb generic ‘pay-for-delay’ deals
References
1. GaBI Online - Generics and Biosimilars Initiative. Pay-to-delay deals up by 60% in US [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2011 September 23]. Available from: www.gabionline.net/Pharma-News/Pay-to-delay-deals-up-by-60-in-US
2. GaBI Online - Generics and Biosimilars Initiative. Authorised generics implicated in pay-to-delay deals [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2011 September 23]. Available from: www.gabionline.net/Pharma-News/Authorised-generics-implicated-in-pay-to-delay-deals
Source: The White House
Research
Positive safety and efficacy primary endpoint results for AVT05 (golimumab proposed biosimilar)
General
Biologicals and biosimilars available for IBD in Canada
Biosimilar medicines on the Pharmaceutical Benefits Scheme in Australia
Most viewed articles
The best selling biotechnology drugs of 2008: the next biosimilars targets
Global biosimilars guideline development – EGA’s perspective
Related content
EMA recommends approval for tocilizumab biosimilar Avtozma and filgrastim biosimilar Zefylti
Ustekinumab biosimilars Yesintek, Steqeyma, and Otulfi approved by FDA, EMA and Health Canada
EMA recommends approval for four denosumab biosimilars: Obodence, Osenvelt, Stoboclo, Xbryk
EMA recommends approval of three aflibercept biosimilars: Ahzantive, Baiama, and Eydenzelt
EMA recommends approval for tocilizumab biosimilar Avtozma and filgrastim biosimilar Zefylti
![Biological 143606710 V14J14ct Biological 143606710 V14J14ct](/var/gabi/storage/images/media/images/biological-143606710-v14j14ct/26301-1-eng-GB/Biological-143606710-V14J14ct_large.jpg)
Biosimilars/News Posted 28/01/2025
Ustekinumab biosimilars Yesintek, Steqeyma, and Otulfi approved by FDA, EMA and Health Canada
![Approved-V13G05 Approved-V13G05](/var/gabi/storage/images/media/images/approved-v13g054/30259-1-eng-GB/Approved-V13G05_large.jpg)
Biosimilars/News Posted 21/01/2025
EMA recommends approval for four denosumab biosimilars: Obodence, Osenvelt, Stoboclo, Xbryk
![Biosimilar biological 800x345 V21L05 Biosimilar biological 800x345 V21L05](/var/gabi/storage/images/media/images/biosimilar-biological-800x345-v21l05/159454-1-eng-GB/biosimilar-biological-800x345-v21l05_large.jpg)
Biosimilars/News Posted 15/01/2025
EMA recommends approval of three aflibercept biosimilars: Ahzantive, Baiama, and Eydenzelt
![02 AA010638 02 AA010638](/var/gabi/storage/images/media/images/02-aa010638/21726-1-eng-GB/02-AA010638_large.jpg)
Biosimilars/News Posted 08/01/2025
The best selling biotechnology drugs of 2008: the next biosimilars targets
![picture09 picture09](/var/gabi/storage/images/media/images/picture09/2207-2-eng-GB/picture09_large.jpg)
Post your comment