FDA backs Roche's Gazyva in first-line follicular lymphoma

Reuters

Thu, Nov 16, 2017, 1:12 PM

ZURICH, Nov 16 (Reuters) - The U.S. Food and Drug Administration on Thursday expanded approvals for Roche's Gazyva to include previously untreated follicular lymphoma, bolstering the Swiss drugmaker's efforts to strengthen its portfolio of blood cancer medicines.

Gazyva is a follow-on drug to Rituxan, which at more than $7 billion in annual sales is Roche's top seller but which has lost patent protection in Europe, exposing it to cheaper copies.

(Reporting by John Miller, editing by David Evans)

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FDA backs Roche's Gazyva in first-line follicular lymphoma

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