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Last kr108.70 SEK
Change Today -1.30 / -1.18%
Volume 883.9K
SOBI On Other Exchanges
As of 11:18 AM 07/1/15 All times are local (Market data is delayed by at least 15 minutes).

swedish orphan biovitrum ab (SOBI) Snapshot

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05/11/15 - kr145.90
52 Week Low
10/16/14 - kr65.25
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swedish orphan biovitrum ab (SOBI) Details

Swedish Orphan Biovitrum AB (publ), an integrated biopharmaceutical company, researches, develops, manufactures, and sells pharmaceuticals in the therapeutic areas of inflammation, and genetics and metabolism diseases primarily in Europe and North America. Its core products include Kineret for the treatment of rheumatoid arthritis and neonatal-onset multisystem inflammatory disease; Orfadin for the treatment of hereditary tyrosinaemia type 1 genetic disorder; Xiapex for the treatment of Peyronie’s disease; and Yondelis for the treatment of a type of cancer. The company also offers Ammonaps, Ammonul, and Ravicti for use in the genetics and metabolism diseases. In addition, it provides Aloxi, Betapred, ChondroCelect, Collatamp, Cometriq, Defibrotide, Erwinase, Ferriprox, Fosinopril, Kepivance, Megestrol, Ruconest, and Willfact for the treatment of rare diseases. Further, the company’s rFVIIIFc and rFIXFc are development projects in pipeline for the treatment of hemophilia; Kiobrina, which is under Phase III clinical trials to enhance growth in premature infants; and SOBI002 is in Phase I clinical trials. It also manufactures drug substance for ReFacto AF/XYNTHA for the treatment of hemophilia A. The company has an agreement with Auxilium Pharmaceuticals for the development, supply, and commercialization of Xiapex, a biologic for the treatment of Dupuytren’s contracture. Swedish Orphan Biovitrum AB (publ) is headquartered in Stockholm, Sweden.

621 Employees
Last Reported Date: 05/6/15

swedish orphan biovitrum ab (SOBI) Top Compensated Officers

Chief Executive Officer and President
Total Annual Compensation: kr5.4M
Compensation as of Fiscal Year 2014.

swedish orphan biovitrum ab (SOBI) Key Developments

Biogen and Swedish Orphan Biovitrum AB (publ) Announce European Medicines Agency Validates Alprolix Marketing Authorization Application

Biogen and Swedish Orphan Biovitrum AB (publ) announced that the European Medicines Agency (EMA) has accepted the Marketing Authorization Application (MAA) of ALPROLIX (rFIXFc), a recombinant factor IX Fc fusion protein product candidate for the treatment of hemophilia B. This validation signifies the initiation of the EMA’s review process. The MAA includes results from two global, Phase 3 clinical trials examining the efficacy, safety and pharmacokinetics (a measure of the presence of the therapy in a person’s body over time) of ALPROLIX for hemophilia B: the pivotal B-LONG study for previously treated adults and adolescents, and Kids B-LONG study for previously treated children under age 12. ALPROLIX is a recombinant, clotting factor IX therapy and is currently approved for the treatment of hemophilia B in the U.S., Canada, Japan and Australia. It is the only approved hemophilia B therapy to demonstrate prolonged clotting factor circulation in the body. Biogen and Sobi are collaborators in the development and commercialization of ALPROLIX for hemophilia B. Sobi has an opt-in right to assume final development and commercialization of ALPROLIX for the Sobi territories (essentially, Europe, North Africa, Russia and certain Middle Eastern markets). Biogen leads development for ALPROLIX, has manufacturing rights, and has commercialization rights in North America and all other regions in the world excluding the Sobi territories.

Swedish Orphan Biovitrum Terminates Takeover Talks

Swedish Orphan Biovitrum AB (OM:SOBI) said that it had terminated discussions regarding a non-binding proposal in relation to a possible offer for the company. The firm said in late April it had received a preliminary proposal for a bid on the company.

Sobi's Partner Biogen Submits Marketing Authorisation Application for Alprolix(R) (rFIXFc) in Europe

Swedish Orphan Biovitrum AB (publ) (Sobi) announced that partner Biogen has submitted a Marketing Authorisation Application (MAA) for Alprolix (rFIXFc) to the European Medicines Agency (EMA). Sobi has an opt-in right to assume final development and commercialisation of Alprolix in Europe, Russia, certain countries in the Middle East, and North Africa. The MAA filing with the EMA coupled with the receipt of the opt-in data package, triggers the formal opt-in right, for Sobi to exercise its option in accordance with the collaboration agreement. Alprolix is a prolonged circulating recombinant factor IX Fc fusion protein product candidate for people with haemophilia B.


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Price/Sales 10.4x
Price/Book 6.5x
Price/Cash Flow 184.8x
TEV/Sales 10.1x

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