Biovitrum Extends ReFacto® Supply Agreement with Wyeth until December 31, 2015

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STOCKHOLM, Sweden and MADISON, New  Jersey, USA - November 12,  2008.
Biovitrum AB (publ) (STO:BVT) and Wyeth (NYSE:WYE) today announced an
extension of the ReFacto® supply  agreement until December 31,  2015.
Biovitrum will continue to be the sole producer of drug substance for
Wyeth for ReFacto®,  as well  as Xyntha®/ReFacto®  AF, the  successor
products, and will continue to receive royalties from Wyeth's  global
sales. Biovitrum's co-promotion  rights in the  Nordic region  remain
unchanged."We are very pleased to be able to announce the prolongation of  our
long and successful collaboration  with Wyeth. The agreement  enables
us to  together provide  the  new improved  Xyntha® and  ReFacto®  AF
internationally, and to  improve the lives  of hemophilia  patients."
commented  Martin  Nicklasson,  CEO  of  Biovitrum.  "The   agreement
validates our biotechnology  therapeutic production capabilities  and
expertise," Nicklasson added.

About ReFacto®, Xyntha® and ReFacto® AF
ReFacto®, Xyntha® and ReFacto® AF  are recombinant protein drugs  for
hemophilia A. In this form of bleeding disorder, the blood's  ability
to coagulate is compromised due to a deficiency of coagulation factor
VIII in the  blood. Uncontrolled internal  bleeding may produce  pain
and swelling  as  well as  permanent  damage, especially  in  joints.
Injections of factor  VIII and  health care allow  most persons  with
hemophilia A to live a normal life.
Market growth for recombinant protein-based drugs to treat hemophilia
A is primarily governed by the transition from plasma-based  products
and an increased acceptance of prophylactic treatment. The market for
recombinant factor VIII used in the treatment of hemophilia A in  the
Nordic regions reached about EUR 80 million in 2007, of which ReFacto
accounted for a market share of about 30 percent.  Biovitrum's  total
revenues from the ReFacto business amounted to SEK 915 in 2007.

ReFacto® AF, approved in the US and Canada under the registered trade
mark Xyntha®,  is manufactured  by  Biovitrum using  next  generation
purification  processes  designed  to   reduce  the  risk  of   viral
contamination, a  production process  completely devoid  of human  or
animal components.



About Biovitrum
Biovitrum is a pharmaceutical company  with operations in Sweden  and
in the UK. The company markets a range of specialist  pharmaceuticals
primarily in the Nordic countries. Using its expertise and experience
Biovitrum takes scientific innovation all  the way to the market  and
to specialist  indication  patients with  significant  medical  need.
Research  expertise   and   capabilities  include   development   and
production of biotechnology therapeutics,  as well as small  molecule
discovery and  development. With  revenues of  approximately SEK  1.3
billion and around 500 employees, Biovitrum is a significant European
specialty pharmaceutical player. Biovitrum's  share is listed on  the
OMX  Nordic  Exchange  in  Stockholm.  For  more  information  go  to
www.biovitrum.com

For more information please contact:

Biovitrum
Martin Nicklasson, CEO
Phone: +46 8 697 2545

Göran Arvidson, CFO
Cell phone: +46 70 633 30 42

Erik Kinnman, VP Investor Relations
Cell phone: +46 73 422 15 40
erik.kinnman@biovitrum.com

Wyeth
Doug Petkus, Wyeth Corporate Media
Phone: +1 973 660 5218

Danielle Halstrom, Wyeth Corporate Affairs
Phone: +1 484 865 2020

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