{"id":302,"date":"2019-10-15T06:12:00","date_gmt":"2019-10-15T04:12:00","guid":{"rendered":"https:\/\/www.ipsen.com\/canada\/?post_type=press_release&p=302"},"modified":"2024-08-21T08:03:01","modified_gmt":"2024-08-21T06:03:01","slug":"health-canada-approves-ipsens-cabometyx-cabozantinib-for-the-first-line-treatment-of-adults-with-advanced-renal-cell-carcinoma","status":"publish","type":"press_release","link":"https:\/\/www.ipsen.com\/canada\/press-releases\/health-canada-approves-ipsens-cabometyx-cabozantinib-for-the-first-line-treatment-of-adults-with-advanced-renal-cell-carcinoma\/","title":{"rendered":"Health Canada Approves Ipsen\u2019s CABOMETYX\u2122 (cabozantinib) for the First-Line Treatment of Adults with Advanced Renal Cell Carcinoma"},"content":{"rendered":"\n
CABOMETYXTM<\/sup> demonstrated a statistically significant, 52 per cent reduction in the risk of progression or death compared with sunitinibi<\/sup>, giving Canadian patients with intermediate or <\/em>poor risk a new oral first-line treatment option in their fight against advanced kidney cancer<\/em><\/strong><\/p>\n\n\n\n Mississauga, ON \u2013 October 15, 2019<\/strong>\u00a0\u2013 Ipsen Biopharmaceuticals Canada Inc. today announced the Health Canada approval of CABOMETYXTM<\/sup>\u00a0(cabozantinib) 20, 40, 60 mg for the first-line treatment of adults with intermediate or poor risk advanced renal cell carcinoma (aRCC), the most common type of kidney cancer.ii<\/sup><\/p>\n\n\n\n \u201cThe Health Canada approval helps strengthen our treatment arsenal for patients with advanced renal cell carcinoma,\u201d says Dr. Anil Kapoor, Professor of Oncology and Surgery at the Juravinski Cancer Centre at McMaster University and Chair of the National Kidney Cancer Research Network of Canada. \u201cIt adds a new option for first line treatment that demonstrated superior clinical efficacy when compared to sunitinib, a current standard of care.\u201d<\/p>\n\n\n\n On average, 7,200 Canadians are diagnosed with kidney cancer each year,iii<\/sup> and the incidence is growing.iv<\/sup> Unfortunately, many kidney cancers are diagnosed at a later stage, or progress to later stages. It is estimated that 1,900 Canadians will die from kidney cancer in 2019, highlighting the need for new treatment options for patients and caregivers.v<\/sup><\/p>\n\n\n\n \u201cA critical goal for many patients is to prolong survival while maintaining quality of life,\u201d says Stephen Andrew, Executive Director of Kidney Cancer Canada. \u201cToday\u2019s announcement is important because it gives patients more options in the fight against the disease.\u201d<\/p>\n\n\n\n This approval was based on the CABOSUN trial which demonstrated that CABOMETYXTM <\/sup>significantly prolonged progression-free survival (PFS) compared to sunitinib in treatment na\u00efve aRCC patients with intermediate or poor-risk disease.vi<\/sup> CABOMETYXTM<\/sup> is the first and only monotherapy to demonstrate superior clinical efficacy over sunitinib in treatment-na\u00efve aRCC patients with intermediate or poor-risk.<\/p>\n\n\n\n \u201cWe come to work every day with the goal of providing hope for patients with difficult-to-treat diseases, and we are thrilled that this expanded indication for CABOMETYXTM<\/sup> widens the scope of patients we can help,\u201d says Ed Dybka, General Manager, Ipsen Canada. \u201cToday\u2019s announcement further demonstrates the efficacy and safety of CABOMETYXTM<\/sup> and reinforces our commitment to expanding its potential across different indications.\u201d<\/p>\n\n\n\n About the CABOSUN Trial<\/strong><\/p>\n\n\n\n CABOSUN was a randomized, open-label, active-controlled phase II study that enrolled 157 patients with aRCC who were intermediate or poor-risk according to International Metastatic RCC Database Consortium (IMDC) criteria as determined by investigator assessment. Patients with previously untreated, locally advanced or metastatic RCC with a clear cell component were randomized (1:1) to receive CABOMETYXTM<\/sup> 60 mg once daily (N=79) or sunitinib 50 mg once daily, four weeks on, followed by two weeks off (N=78); The primary efficacy endpoint was PFS retrospectively assessed by a blinded Independent Radiology Committee (IRC). Secondary endpoints included overall survival (OS) and objective response rate (ORR).vii<\/sup><\/p>\n\n\n\n In the trial, CABOMETYXTM<\/sup> demonstrated a clinically meaningful and statistically significant reduction in the rate of disease progression or death as measured by PFS. Median PFS for CABOMETYX in the Independent Review Committee (IRC) assessment was 8.6 months versus 5.3 months for sunitinib (HR=0.48, 95% CI, p=0.0008).viii<\/sup> The most common adverse reactions in \u2265 10% of CABOMETYXTM<\/sup> treated patients were diarrhea, hypertension, fatigue and increased levels of aspartate aminotransferase.ix<\/sup><\/p>\n\n\n\n About CABOMETYXTM<\/sup>\u00a0(cabozantinib)<\/strong><\/p>\n\n\n\n CABOMETYXTM<\/sup> is the first multi-targeted tyrosine kinase inhibitor (TKI) to target VEGFR, MET and AXL pathways that are involved in tumour progression in RCC. It works by blocking the action of proteins called receptor tyrosine kinases (RTKs). RTKs are involved in cell growth and the development of new blood vessels. These proteins can be present in high amounts in cancer cells. By blocking their action, CABOMETYXTM<\/sup> can slow down how fast the tumour grows, help to block the blood supply that the cancer needs and may increase the length of time before the cancer gets worse.x<\/sup><\/p>\n\n\n\n Following a priority review by Health Canada, CABOMETYXTM <\/sup>was first approved in Canada in September 2018 for the treatment of adult patients with aRCC who had received prior VEGFtargeted therapy.xi<\/sup><\/p>\n\n\n\n About Ipsen<\/strong><\/p>\n\n\n\n Ipsen Biopharmaceuticals Canada Inc., the Canadian affiliate of Ipsen, is headquartered in Mississauga, Ontario with established operations since October 2015.\u00a0 For more information on Ipsen Biopharmaceuticals Canada Inc. visit\u00a0www.ipsen.ca<\/strong><\/a>.<\/a>\u00a0 Ipsen is a global specialty-driven biopharmaceutical group focused on innovation and specialty care. The group develops and commercializes innovative medicines in three key therapeutic areas \u2013 Oncology, Neuroscience and Rare Diseases. Its commitment to Oncology is exemplified through its growing portfolio of key therapies for prostate cancer, neuroendocrine tumors, renal cell carcinoma and pancreatic cancer. Ipsen\u2019s R&D is focused on its innovative and differentiated technological platforms located in the heart of the leading biotechnological and life sciences hubs (Paris-Saclay, France; Oxford, UK; Cambridge, US). The Group has about 5,700 employees worldwide. Ipsen is listed in Paris (Euronext: IPN) and in the United States through a Sponsored Level I American Depositary Receipt program (ADR: IPSEY). For more information on Ipsen, visit\u00a0www.ipsen.c<\/strong><\/a>om<\/strong>.<\/a><\/p>\n\n\n\n For further information:<\/strong><\/p>\n\n\n\n