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Durata seeks FDA OK for dalbavancin in ABSSSI

This article was originally published in Scrip

Executive Summary

Shares of Durata Therapeutics rose as much as 3.6% on 27 September on the news the company is seeking the FDA's approval to market dalbavancin as a treatment for patients with acute bacterial skin and skin structure infections (ABSSSI) caused by susceptible Gram-positive microorganisms, including methicillin resistant Staphylococcus aureus (MRSA).

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