S-P withdraws Cylatron MAA
US drug major Schering-Plough has withdrawn its application for a centralized marketing authorization for Cylatron (peginterferon alfa-2b), 200mcg/0.5ml, 300mcg/0.5ml and 600mcg/ml.
The agent was expected to be used for the adjuvant treatment of patients with stage III melanoma as evidenced by microscopic, non-palpable nodal involvement.
The application for the marketing authorization for Cylatron was submitted to the EMEA on September 7, 2007. At the time of the withdrawal, it was under review by the Agency's Committee for Medicinal Products for Human Use (CHMP).
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