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Prexige Review Will Not Include FDA Arthritis Drugs Advisory Committee

This article was originally published in The Pink Sheet Daily

Executive Summary

Novartis expects action later this year on lumiracoxib after resubmitting the application, the company tells “The Pink Sheet” DAILY.

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Novartis Withdraws Prexige In Australia Ahead Of FDA Decision Due To Deaths

Withdrawal of the COX-2 inhibitor in Australia following two deaths from liver injury is likely to impact the outcome of FDA’s review.

Novartis Withdraws Prexige In Australia Ahead Of FDA Decision Due To Deaths

Withdrawal of the COX-2 inhibitor in Australia following two deaths from liver injury is likely to impact the outcome of FDA’s review.

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