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EMA accepts Pfizer’s filing for regulatory review of axitinib for patients with advanced RCC
New York | Friday, June 3, 2011, 14:00 Hrs  [IST]

Pfizer Inc. announced that the European Medicines Agency (EMA) has accepted Pfizer’s filing for regulatory review of axitinib for patients with advanced Renal Cell Carcinoma (RCC) after failure of prior systemic treatment. This submission was based on phase III data from the AXIS 1032 trial. Pfizer will present full results from this trial, as well as additional data on axitinib, at the 47th Annual Meeting of the American Society of Clinical Oncology (ASCO), being held in Chicago from June 3-7, 2011.

“While the prognosis for patients with advanced RCC has improved dramatically over the past five years thanks to the availability of new treatments, there is still a need for new options in this patient population,” said Garry Nicholson, president and general manager, Pfizer Oncology Business Unit. “This regulatory filing for our innovative investigational therapy axitinib, as well as ongoing studies of our existing medications, underscores Pfizer’s commitment to patients with advanced RCC and our leadership in helping physicians treat this disease.”

Each year, approximately 210,000 people worldwide are diagnosed with kidney cancer and nearly 102,000 people are expected to die from the disease. Within the last five years, great advances have been made in the treatment of patients with advanced RCC, the most prevalent form of kidney cancer. However, five-year survival rates for patients with advanced RCC remain low, at around 20 percent.

Axitinib is an oral and selective inhibitor of Vascular Endothelial Growth Factor (VEGF) receptors 1, 2 and 3, receptors that can influence tumor growth, vascular angiogenesis and progression of cancer (the spread of tumors). Axitinib is an investigational agent that has not been approved by regulatory agencies in any countries or jurisdictions.

Axitinib is also being investigated in a randomized Phase III clinical trial in patients with treatment-naïve as well as previously treated advanced RCC, and in a randomized phase II clinical trial for the treatment of Hepatocellular Carcinoma (HCC).

As a leader in the treatment of advanced RCC, Pfizer Oncology is dedicated to offering multiple treatments and investigating new agents in different populations and stages of disease. Pfizer’s RCC portfolio offers two approved therapies for the treatment of people with advanced RCC. By working collaboratively with academic institutions, individual researchers, cooperative research groups, governments, licensing partners and people affected, we are committed to advancing the science of RCC through research into established and novel compounds, as well as the exploration of biomarkers to better personalize therapy.

Pfizer Oncology is committed to the discovery, investigation and development of innovative treatment options to improve the outlook for cancer patients worldwide.

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