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THRX > SEC Filings for THRX > Form 8-K on 18-Mar-2014All Recent SEC Filings

Show all filings for THERAVANCE INC



Other Events

Item 8.01 Other Events.

On March 17, 2014, Theravance, Inc. ("Theravance") was informed by its partner, Clinigen Group plc ("Clinigen") that it had received a notification dated March 13, 2014 from the European Commission (EC) that the EC has lifted the Europe-wide suspension of Marketing Authorization and amended the Marketing Authorization for VIBATIV® (telavancin) for the treatment of adults with nosocomial pneumonia (hospital-acquired), including ventilator-associated pneumonia, known or suspected to be caused by methicillin resistant Staphylococcus aureus (MRSA) when other alternatives are not suitable. Theravance and Clinigen have an exclusive commercialization agreement in the European Union and certain other European countries (including Switzerland and Norway) for VIBATIV®.

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