Arpida A/S Withdraws Its Marketing Authorisation Application For Mersarex (iclaprim), Europe

Main Category: Dermatology
Also Included In: Regulatory Affairs / Drug Approvals
Article Date: 25 Oct 2009 - 0:00 PDT

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The European Medicines Agency has been formally notified by Arpida A/S of its decision to withdraw its application for a centralised marketing authorisation for the medicine Mersarex (iclaprim), 12.8 mg/ml concentrate for solution for infusion.

Mersarex was expected to be used for the treatment of complicated skin and soft tissue infections.

The application for the marketing authorisation for Mersarex was submitted to the Agency on 25 July 2008. At the time of the withdrawal, it was under review by the Agency's Committee for Medicinal Products for Human Use (CHMP).

In its official letter, the company stated that the withdrawal of the application was based on the CHMP's view that the data provided did not allow the Committee to conclude on a positive benefit-risk balance for Mersarex.

More information about Mersarex and the state of the scientific assessment at the time of withdrawal will be made available in a question-and-answer document. This document, together with the withdrawal letter from the company, will be published on the Agency's website after the next CHMP meeting of 16-19 November 2009.

Notes

1. Withdrawal of an application does not prejudice the possibility of a company making a new application at a later stage.

Source
EMEA

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