News
14 Mar 2012
Alkermes Pharma Withdraws Marketing Authorisation Application for Megestrol Alkermes
Alkermes Pharma stated in its official letter that the decision to withdraw the application was a consequence of portfolio prioritisation.
The European Medicines Agency has been formally notified by Alkermes Pharma Ireland Limited of its decision to withdraw its application for a centralised marketing authorisation for the medicine Megestrol Alkermes (megestrol), 125 mg/ml oral suspension.
The drug was intended to be used for the treatment of anorexia, cachexia or an unexplained significant weight loss in adult AIDS and oncology patients.
Alkermes Pharma stated in its official letter that the decision to withdraw the application was a consequence of portfolio prioritisation.
The application for the marketing authorisation for
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