Patients in Manitoba and Saskatchewan living with the most common form of leukemia[1] now have access to a targeted treatment option

GAZYVA® to be reimbursed in Manitoba and Saskatchewan for patients with Chronic Lymphocytic Leukemia

MISSISSAUGA, ON, July 6, 2015 /CNW/ - People in Manitoba and Saskatchewan living with Chronic Lymphocytic Leukemia (CLL) will now be able to access a new treatment option through the prescription drug insurance plans in both provinces. Earlier this week, GAZYVA® (obinutuzumab) in combination with chlorambucil chemotherapy was added to benefits formularies of the Provincial Oncology Drug Programs at CancerCare Manitoba and the Saskatchewan Cancer Agency. These decisions follow the announcement on June 2, 2015 that the treatment would be funded in Quebec.

"We are pleased to hear that GAZYVA® will be made available to CLL patients in Manitoba and Saskatchewan," said Mr. Ronnie Miller, president and CEO, Roche Canada. "The inclusion of GAZYVA® on these provincial formularies means that more CLL patients will have access to this important new treatment option."

CLL is the most common form of adult leukemia, with nearly 2,200 Canadians diagnosed each year.2,3 It is an incurable, slow-growing cancer of the blood and bone marrow.4 Since the average age of diagnosis for CLL is 72 years, nearly 90 per cent of patients are living with at least one comorbidity (e.g., cardiac disease, diabetes or respiratory disease), which may be associated with their age and lifestyle, potentially limiting their treatment options.5

CLL is a blood cancer that causes "B-lymphocyte" cells to multiply too quickly and live too long. GAZYVA® works by binding to the surface of these cells, causing them to die.6

GAZYVA® was approved by Health Canada on November 25, 2014, in combination with chlorambucil, for the treatment of patients with previously untreated CLL.7 The treatment is now funded in Manitoba, Saskatchewan and Quebec, but continues to be under review in all other Canadian provinces.

GAZYVA® is a monoclonal antibody designed to bind to CD20, a protein found on white blood cells called B cells. It attacks targeted cells both directly and together with the body's immune system. GAZYVA® was designed by Roche Glycart AG, a wholly-owned, independent research unit of Roche and is the first medicine approved under the U.S. Food and Drug Administration's (FDA) Breakthrough Drug designation.8 GAZYVA® is also approved as a first-line treatment for CLL by the European Commission under the brand name GAZYVARO™.

Health Canada's approval of GAZYVA® is based on results from the pivotal Phase III CLL11 trial, which was a multicenter, open-label, randomized three-arm study enrolling 781 patients with previously untreated CLL and co-existing medical conditions.

The CLL11 trial was conducted in cooperation with the German CLL Study Group (GCLLSG) and investigated the efficacy, as well as safety profile of either GAZYVA® plus chlorambucil or RITUXAN® (rituximab) plus chlorambucil compared to chlorambucil alone. The trial showed that people who received GAZYVA® in combination with chlorambucil significantly reduced the risk of disease progressions or death by 84 per cent compared to chlorambucil alone (HR=0.16; p<0.0001). GAZYVA® also more than doubled the time people with newly diagnosed CLL lived without the disease getting worse (median progression-free survival (PFS): 23.0 months vs. 11.1 months). Approximately one in five patients (or 22 per cent) receiving GAZYVA® in combination with chlorambucil achieved a complete response (CR), which is the disappearance of all signs of cancer in response to treatment.9

The most common Grade 3/4 adverse events for those who received GAZYVA® in combination with chlorambucil compared to chlorambucil alone were infusion-related reactions during the first infusion (21 per cent vs. 0 per cent [chlorambucil is an oral medicine]), low platelet count (thrombocytopenia, 11 per cent vs. 3 per cent) and low count of certain types of white blood cells (neutropenia, 34 per cent vs. 16 per cent).10

About Roche
Headquartered in Basel, Switzerland, Roche is a leader in research-focused healthcare with combined strengths in pharmaceuticals and diagnostics. Roche is the world's largest biotech company, with truly differentiated medicines in oncology, infectious diseases, inflammation, metabolism and neuroscience. Roche is also the world leader in in vitro diagnostics and tissue-based cancer diagnostics, and a frontrunner in diabetes management. Roche's personalized healthcare strategy aims at providing medicines and diagnostic tools that enable tangible improvements in the health, quality of life and survival of patients. In 2012 Roche had over 82,000 employees worldwide and invested over 8 billion Swiss francs in R&D. The Group posted sales of 45.5 billion Swiss francs. Genentech, in the United States, is a wholly owned member of the Roche Group. Roche is the majority shareholder in Chugai Pharmaceutical, Japan. For more information, please visit

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Disclaimer: Cautionary statement regarding forward-looking statements
This document may contain certain forward-looking statements. These forward-looking statements may be identified by words such as 'believes', 'expects', 'anticipates', 'projects', 'intends', 'should', 'seeks', 'estimates', 'future' or similar expressions or by discussion of, among other things, strategy, goals, plans or intentions. Various factors may cause actual results to differ materially in the future from those reflected in forward-looking statements contained in this document, among others: (1) pricing and product initiatives of competitors; (2) legislative and regulatory developments and economic conditions; (3) delay or inability in obtaining regulatory approvals or bringing products to market; (4) fluctuations in currency exchange rates and general financial market conditions; (5) uncertainties in the discovery, development or marketing of new products or new uses of existing products, including without limitation negative results of clinical trials or research projects, unexpected side effects of pipeline or marketed products; (6) increased government pricing pressures; (7) interruptions in production; (8) loss of or inability to obtain adequate protection for intellectual property rights; (9) litigation; (10) loss of key executives or other employees; and (11) adverse publicity and news coverage. The statement regarding earnings per share growth is not a profit forecast and should not be interpreted to mean that Roche's earnings or earnings per share for any current or future period will necessarily match or exceed the historical published earnings or earnings per share of Roche.



The Leukemia and Lymphoma Society of Canada. Disease information and support. Accessed June 24, 2015.


The Leukemia and Lymphoma Society of Canada. Disease information and support. Accessed on June 24, 2015.


Canadian Cancer Society. Chronic Lymphocytic Leukemia. Chronic lymphocytic leukemia statistics. Accessed June 24, 2015.


Canadian Cancer Society. Chronic Lymphocytic Leukemia. Disease progression of chronic lymphocytic leukemia. Accessed June 24, 2015.


Thurmes P, Call T, Slager S, et al. Comorbid conditions and survival in unselected, newly diagnosed patients with chronic lymphocytic leukemia. Leuk Lymphoma. 2008;49(1):49-56.


GAZYVA® Product Monograph. November 25, 2014.


GAZYVA® Product Monograph. November 25, 2014.


U.S. Food and Drug Administration. (2013). FDA approves Gazyva for chronic lymphocytic leukemia [Press release]. Accessed June 24, 2015. 


Goede V, Fischer K, Busch R, et al. Obinutuzumab plus Chlorambucil in Patients with CLL and Coexisting Conditions. N Engl J Med. 2014 Mar 20;370(12):1101-10.


GAZYVA® Product Monograph. November 25, 2014.

SOURCE Roche Canada

For further information: Kate Hanna, Roche Canada, 905-285-7729,; Alexa Vogel, Edelman, 416-850-0387,

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