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Janssen submits supplemental application to FDA for Edurant

Johnson & Johnson’s Janssen Pharmaceutical announced the submission of a supplemental new drug application to the Food and Drug Administration seeking to expand the indication of Edurant to include the treatment of HIV-1 infection in children weighing 10 kg or more. A parallel marketing authorization application has also been submitted to the European Medicines Agency in support of a type II variation and line extension for expanded pediatric use in Europe.

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