Positioning of biosimilars: commodity versus differentiated

INICIO/Informes | Posted 24/08/2012 post-comment2 Post your comment

How to market a new biosimilar is a key question, especially when taking into consideration the costs that are associated with developing a biosimilar. Whether the biosimilar will be a bulk (commodity) product or a differentiated product can have significant impact on the uptake of the biosimilar.


Uptake of biosimilars varies between different countries when therapy areas are considered according to drug class [1]. For example, the market for somatropin is differentiated due to a complex stakeholder landscape influenced by physicians, the competition is based on multiple marketing levers. This results in uptake of biosimilar somatropin being significantly lower than in commodity markets where access is mostly controlled by payers, e.g. tender, step-wise algorithms; and price competition, e.g. G-CSF, epoietins. Differentiated biosimilars are most likely when they are indicated for chronic treatment and/or long therapeutic cycles, where patients prefer to stick to a ‘known’ product. On the other hand, commodity biosimilars are most likely those indicated for acute treatment and/or frequent cycling among therapies.

Just looking at five of the biosimilars that have entered the regional markets or due to enter the global market in the coming years, you can find both commodity and differentiated products amongst them, see Figure 1.

Figure 1: Positioning of current and future biosimilars [1]

GW 1082G 5 figure 1

Uptake patterns will most likely vary across geographic clusters, and, for example, biosimilar insulins may perform better in emerging countries, such as Brazil, China,

India and Mexico. These countries have already developed their own regulatory pathways to manage the approval of biosimilars, with in general lower barriers in terms of clinical trial requirements and regulatory control than in Europe.

Editor’s comment
If you would like to receive figure 1* with added information on 12 forthcoming biosimilars, please send us an email.

*For profit organisations subjected to a fee

Related articles

Future biosimilar targets

European uptake of biosimilars

Global uptake of biosimilars

Biosimilars: key players and global market trends


1.  Sheppard A. Iervolino A. Biosimilars: about to leap. 10th EGA International Symposium on   Biosimilar Medicines; 2012 Apr 19; London, UK.

Permission granted to reproduce for personal and educational use only. All other reproduction, copy, retransmission 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.

comment icon Comments (2)
Post your comment
Posted 20/09/2012 by Lasia, GaBI Online Editorial Office
Response to 'Commodity versus differentiated'

Dear Mr Swit,
Thank you for your comments. The interchangeability of biosimilars is under discussion. The 'Commodity' market has several criteria in order to make it work. We will publish a Biosimilars educational series (http://gabi-journal.net/gabi-journal/about-gabi-journal/future-activities/educational-book-series) and the topic of 'interchangeability' will be addressed.
Best regards,
Lasia, Publisher, GaBI Online

Posted 24/08/2012 by Michael A. Swit
Commodity versus differentiated

In the United States, under the emerging regime created by the Biosimilars Price Competition and Innovation Act, absent a finding of interchangeability, do you envision any non-interchangeable biosimilar ever being truly a commodity? Perhaps I am being semantical, but I do not see how a commodity market can emerge in that situation.

Most viewed articles
Sobre GaBI
INICIO/Sobre GaBI Posted 06/08/2009
EU guidelines for biosimilars
EMA logo 1 V13C15
INICIO/Directrices Posted 08/10/2010