Sandoz Canada gets approval to launch oncology biosimilars Ziextenzo, Riximyo
Sandoz Canada received a Notice of Compliance from Health Canada on April 21, 2020, for the use of Ziextenzo to reduce the incidence of febrile neutropenia, one of the most serious side effects of chemotherapy. Riximyo was approved on April 28, 2020, to treat non-Hodgkin's lymphoma, chronic lymphocytic leukemia, and rheumatoid arthritis.;
Boucherville: Sandoz Canada Inc., a division of Novartis AG, has announced that Health Canada has approved Ziextenzo (pegfilgrastim, reference biologic drug: Neulasta) and Riximyo (rituximab, reference biologic drug: Rituxan) for marketing in Canada.
Sandoz Canada received a Notice of Compliance from Health Canada on April 21, 2020, for the use of Ziextenzo to reduce the incidence of febrile neutropenia, one of the most serious side effects of chemotherapy. Riximyo was approved on April 28, 2020, to treat non-Hodgkin's lymphoma, chronic lymphocytic leukemia, and rheumatoid arthritis.
Neutropenia is a decrease in the number of neutrophils, a type of white blood cell, which predisposes the body to infections and prevents it from fighting them.
According to statistics published by the Canadian Cancer Society, in 2019 an estimated 21,000 Canadians received a blood cancer diagnosis, which makes up approximately 10% of all cancer diagnoses and includes non-Hodgkin's lymphoma (10,000) and leukemia (6,700). Survival rates for blood cancers have increased over the years, but they still caused the deaths of 7,200 Canadians in 2016, according to a report released by The Leukemia & Lymphoma Society of Canada.
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