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12 Current news of Shire

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Heptares grants Shire an exclusive worldwide license to develop and commercialise drug candidates for CNS disorders

03-22-2012

Heptares Therapeutics announced that an operating company of Shire plc has exercised its exclusive option to license a novel adenosine A2A antagonist discovered by Heptares that is currently in preclinical development. Adenosine A2A is a G-protein coupled receptor (GPCR) involved in the ...

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arGEN-X enters into therapeutic antibody alliance with Shire

03-02-2012

arGEN-X announced that it has entered into an alliance with Shire to create novel therapeutic antibody products against multiple targets submitted by Shire. Using its SIMPLE Antibody™ discovery technology, arGEN-X will isolate and characterize human antibodies against the targets that Shire ...

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Shire Presents Positive Data from Fabry and Gaucher Disease Studies that Continue to Support Patient Switches to REPLAGAL and VPRIV

09-01-2011

Shire plc announced positive data from several studies designed to evaluate the safety of switching to REPLAGAL (agalsidase alfa) from Fabrazyme® (agalsidase beta) and the long-term safety and benefits of switching to VPRIV (velaglucerase alfa) from Cerezyme® (imiglucerase). Study results are ...

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Shire Announces European Approval of VPRIV (velaglucerase alfa) for the Treatment of Type 1 Gaucher Disease

08-30-2010

Shire plc announced that the European Commission has granted marketing authorisation for VPRIV(R) (velaglucerase alfa), a human cell line derived enzyme replacement therapy (ERT) for the long-term treatment of type 1 Gaucher disease. VPRIV has been authorized as an orphan medicine through the ...

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Shire Receives Fast Track Designation for velaglucerase alfa for Gaucher Disease

07-17-2009

Shire plc announces it has received Fast Track designation from the U.S. Food and Drug Administration (FDA) for velaglucerase alfa, its enzyme replacement therapy in development for the treatment of Type I Gaucher disease. Shire is working with the FDA to determine subsequent steps and timing ...

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Strategic Review of Jerini Assets Completed

10-13-2008

Jerini AG and Shire Deutschland Investments GmbH have completed the strategic review of the assets and programs of Jerini AG, not related to Icatibant (Firazyr®), as referred to in the Offer Document published by Shire Deutschland Investments GmbH on August 13, 2008. The Jerini Supervisory ...

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Change of Name to Shire plc

10-06-2008

Shire Limited announces that following the approval by shareholders at the Annual General Meeting on September 24, 2008, the Company has changed its name to Shire plc with effect from today. Shire plc's ticker symbols on the London Stock Exchange and NASDAQ and the ISIN numbers of the ...

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Jerini sells onself to british Shire

Jerini AG for an equity purchase price of EUR 328 million

07-07-2008

Shire Limited, the global specialty biopharmaceutical company, announced that Maia Elfte Vermögensverwaltungs-GmbH, to be renamed "Shire Deutschland Investments GmbH", a German indirect subsidiary of Shire Limited, will launch a voluntary public takeover offer for shares in Jerini AG, the ...

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FDA Advisory Committee Votes in Favor of Earlier Use of Phosphate Binders in Stage 4 Kidney Disease Patients

10-18-2007

At the U.S. Food and Drug Administration's (FDA's) Cardiovascular and Renal Drugs Advisory Committee meeting, the majority of members voted to recommend the use of phosphate binders, including Shire Pharmaceuticals' non-calcium FOSRENOL(R) (lanthanum carbonate), to treat hyperphosphatemia ...

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Innovative technology for treatment of renal anaemia

First human cell line-derived erythropoietin research reported

06-20-2006

Effective treatment of anaemia in patients suffering from chronic kidney disease (CKD) is possible with the first erythropoietin product produced in a human cell line. DYNEPO® (epoetin delta), developed using innovative gene activation technology in a human cell line, corrects and maintains ...

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