On 2 May 2011, Teva and Cephalon announced that they had unanimously approved a definitive agreement under which Teva will acquire all outstanding shares of Cephalon for US$81.50 per share in cash, or a total enterprise value of approximately US$6.8 billion.
Teva grabs biopharmaceutical company Cephalon
Biosimilars/News
|
Posted 06/05/2011
0
Post your comment
![picture 99 picture 99](/var/gabi/storage/images/media/images/picture-99/7981-1-eng-GB/picture-99_large.jpg)
Teva beat Valeant to the post by offering 6% above Valeant’s offer. The deal not only increases Teva’s branded business, but also enhances its generic presence in high growth emerging markets. The deal includes Mepha, Cephalon’s generics unit, which is the generics leader in Switzerland and which has a geographic presence in Africa, Central and Eastern Europe, and Latin America.
It is no wonder that Teva is making sure it has a firm foothold in the biopharmaceutical business. In 2009, biologicals sales reached US$130 billion. Cephalon’s branded portfolio currently represents approximately US$7 billion in sales, with a robust ‘pipeline’ including more than 30 late-stage compounds.
Since Teva is undoubtedly the world’s number one generics company and is, as it puts it, ‘commitment to providing consumers with access to high-quality, affordable medicines’, one can only speculate that this acquisition may also be used to reinforce its presence in the biosimilars market.
It is estimated that, by 2015, US$60 billion-worth of biologicals will lose patent protection. Teva already has a biosimilar granulocyte colony-stimulating factor approved in the EU, with a low molecular weight heparin, a biosimilar version of Lovenox (enoxaparin sodium), awaiting approval. Meanwhile, it is working on a biosimilar version of Roche’s blood-cancer drug, Rituxan (rituximab).
Related articles
Generics manufacturers and biosimilars
Spectrum to develop biosimilar monoclonal antibody
Source: Cephalon, Teva
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