Obstacles to the use of biosimilars in the US

Generics and biosimilars Initiative

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Obstacles to the use of biosimilars in the US

Biosimilares/Investigación | Posted 13/04/2018 0 Post your comment

Professor Richard G Frank from the Department of Health Care Policy, Harvard Medical School, Boston, USA, discusses factors that may account for the slow development of competition in the market for biosimilars in the US [1].

An abbreviated pathway for biosimilars was signed into law as part of the Affordable Care Act in 2010 [2]. However, it took five years before the US Food and Drug Administration (FDA) approved its first biosimilar, Zarxio (filgrastim-sndz) in March 2015 [3]. To date, the agency has approved nine biosimilars, of which only seven are on the US market. This compares with Europe, which created a biosimilars pathway in 2005/2006 and had already approved its first biosimilar Omnitrope (somatropin) in April 2006 [4]. There were also 14 biosimilars on the European market at a similar point in time after a pathway was created.

Professor Frank highlights factors, including naming, interchangeability guidance, insurance payment arrangements and secrecy about manufacturing processes; that probably account for the slow development of competition in the US biologicals market.

He points out that although the factors separately may only have modest effects, ‘together they are additive and most likely contribute to the slow development of competition in the biologic[al]s market’ in the US.

It is estimated that currently, only US$3.2 billion (3%) of US spending on biologicals is subject to competition from biosimilars. With spending on biologicals estimated to be US$105.5 billion in 2016 and increasing by an average 10% per year, there are huge potential savings to be made with increased use of biosimilars.

The factors are discussed in more detail in the series of four articles that follow.

Conflict of interest
Disclosure forms provided by the author [1] are available at NEJM.org.

Insurance payment arrangements are an obstacle to biosimilars use in the US

Interchangeability is an obstacle to the use of biosimilars in the US

Naming is an obstacle to the use of biosimilars in the US

References
1. Frank RG. Friction in the path to use of biosimilar drugs. N Engl J Med. 2018;378(9):791-3.
2. GaBI Online - Generics and Biosimilars Initiative. When will the US biosimilars pathway be used [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2018 Apr 13]. Available from: www.gabionline.net/Biosimilars/News/When-will-the-US-biosimilars-pathway-be-used
3. GaBI Online - Generics and Biosimilars Initiative. Biosimilars approved in the US [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2018 Apr 13]. Available from: www.gabionline.net/Biosimilars/General/Biosimilars-approved-in-the-US
4. GaBI Online - Generics and Biosimilars Initiative. Biosimilars approved in Europe [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2018 Apr 13]. Available from: www.gabionline.net/Biosimilars/General/Biosimilars-approved-in-Europe

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