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FDA OKs subcutaneous formulation of Roche's Rituxan for certain blood cancers

Published 06/22/2017, 03:51 PM
Updated 06/22/2017, 03:51 PM
© Reuters.  FDA OKs subcutaneous formulation of Roche's Rituxan for certain blood cancers
  • The FDA approves Roche's (OTCQX:RHHBY) RITUXAN HYCELA (rituximab and hyaluronidase human) for subcutaneous injection for the treatment of three blood cancers: (all previously untreated) follicular lymphoma, diffuse large B-cell lymphoma and chronic lymphocytic leukemia.
  • The product includes the same monoclonal antibody as the intravenous formulation and combines it with an enzyme that helps deliver it under the skin.
  • U.S. commercial launch will commence in a week or two.
  • Now read: Allergan (NYSE:AGN) - A Positive Outlook And A Nice Catalyst 4 Months Away


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