PARIS, June 4, 2011 /PRNewswire/ --
- Results of Phase III SAVE-ONCO Study Selected for "Best of ASCO 2011" -
- Venous Thrombo-embolism Affects Up to 1 in 5 Cancer Patients And Chemotherapy Further Increases this Risk
Sanofi (EURONEXT: SAN and NYSE: SNY) announced today results of the pivotal SAVE-ONCO study which demonstrated that, in cancer patients initiating a chemotherapy regimen, investigational semuloparin significantly reduced the risk of the composite of symptomatic-deep vein thromboembolism (DVT), non-fatal pulmonary embolism (PE) or venous thromboembolism (VTE)-related death by 64%[i], meeting the study primary endpoint (respectively 1.2% and 3.4% for semuloparin and placebo HR 0.36 95% CI (0.21-0.60)), p< 0.0001). Semuloparin reduced the risk of this type of blood clots without increasing the incidence of major bleeding over placebo (1.2% vs. 1.1%) [i]. The SAVE-ONCO study results will be presented on June 6, 2011 in an oral presentation at the 47th Annual Meeting of the American Society of Clinical Oncology (ASCO) in Chicago, and are selected for the Best of ASCO*.
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In VTE, blood clots usually form in deep veins (commonly referred as thrombo-phlebitis) and can migrate and potentially block blood flow in the blood vessels of the lungs (pulmonary embolism), which may result in sudden death [ii]. Often clinically silent, VTE is a life-threatening complication of cancer affecting up to one in five patients[iii], [iv], and initiating chemotherapy further increases the risk by more than 60%[v],[vi].
"For cancer patients initiating chemotherapy, there is currently no approved treatment for the primary prevention of venous thrombo-embolism risk," said Giancarlo Agnelli, Professor of Internal Medicine at the University of Perugia, Italy and SAVE-ONCO principal study investigator. "Therefore, we are encouraged by the 64% risk reduction of Life-Threatening Venous Blood Clots demonstrated in this randomized trial".
"In many patients affected by cancer, preventing venous thromboembolism is an important clinical management issue", said Dr. Elias Zerhouni, President, Global Research & Development, Sanofi. "We are pleased with the results achieved in this study of our selectively engineered semuloparin as shown by the SAVE-ONCO trial. Based on these results of SAVE-ONCO we plan to submit semuloparin for regulatory filing in Q3 2011".
SAVE-ONCO, the international randomized phase 3 study enrolled 3,212 patients initiating a chemotherapy regimen for locally advanced or metastatic solid tumor (lung, colon-rectum, stomach, ovary, pancreas or bladder cancer). Patients received either a daily 20 mg subcutaneous administration of semuloparin or placebo for at least three months or until change in the chemotherapy regimen. The primary endpoint of the study was the composite of any symptomatic-DVT, non-fatal PE and VTE-related deathi. Clinically relevant bleeding (bleedings requiring medical attention) was respectively 2.8% and 2.0% for semuloparin and placeboi . Consistent with previous findings, there was no case of reported HIT (heparin induced thrombocytopenia) in the 3,212 studied patients. SAVE-ONCO study median treatment duration with semuloparin was approximately 3.5 monthsi.
* The 2011 Best of ASCO Meetings feature the most relevant and cutting-edge science in oncology research.
Semuloparin is an investigational selectively engineered Ultra-LMWH (low molecular weight heparin) with enriched anti-thrombin binding sites, leading to anticoagulant activity mainly directed towards coagulation Factor Xa, with a minimal effect on Factor IIa. Selectively engineered semuloparin, in addition to a specific anti-Factor Xa/IIa ratio, retains biological activities that are relevant in cancer biology such as effects on TFPI (tissue factor pathway inhibitor)[vii]. A large Phase III clinical study (SAVE-ONCO) investigating semuloparin benefit in cancer patients with locally advanced or metastatic solid tumor initiating chemotherapy has been completed. The SAVE-ONCO study assessed the efficacy and safety of semuloparin for the prevention of symptomatic- DVT, non-fatal Pulmonary Embolism and VTE-related death in cancer patients initiating a chemotherapy regimen.
About Sanofi Oncology
Based in Cambridge, Massachusetts, and Vitry, France, Sanofi Oncology is dedicated to translating science into effective cancer therapeutics to address unmet medical needs for patients with cancer. Starting with a deep understanding of the mechanisms by which cancer develops, grows and spreads, the company employs innovative approaches in drug discovery, clinical development and partnerships to bring the right medicines to the right patients with the goal of helping cancer patients live healthier and longer lives.
Sanofi Oncology is committed to the pursuit of science and innovative cancer therapies. We believe in partnership with leading experts, and combining that expertise with our own internal scientific strength and heritage. There are currently more than 10 investigational compounds in clinical development including small molecules and biological agents.
Sanofi, a global and diversified healthcare leader, discovers, develops and distributes therapeutic solutions focused on patients' needs. Sanofi has core strengths in the field of healthcare with seven growth platforms: diabetes solutions, human vaccines, innovative drugs, rare diseases, consumer healthcare, emerging markets and animal health. Sanofi is listed in Paris (EURONEXT: SAN) and in New York (NYSE: SNY).
Forward Looking Statements
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[i] Agnelli G et al. ASCO June 3-7, 2011 Chicago. Oral Abstract #LBA9014.
[ii] Heit AJ. Risk factors for venous thromboembolism. Clin Chest Med. 2003 Mar; 24 (1): 1-12.
[iii] Lyman GH. Venous Thromboembolism in the Patient With Cancer. Cancer 2011; 1334-50.
[iv] Khorana AA et al. Thromboembolism is a leading cause of death in cancer patients receiving outpatient chemotherapy . J Thromb Haemost 2007;5:632-4.
[v] Heit JA. Cancer and Venous Thromboembolism: Scope of the Problem. Cancer Control. September 2005; 12: 5-10.
[vi] Heit JA et al. Risk Factors for Deep Vein Thrombosis and Pulmonary Embolism. Arch Intern Med 2000 ;160:809-15.
[vii] Gómez-Outes A et al. New parenteral anticoagulants in development. Ther Adv Cardiovasc Dis 2011 5: 33-59.Video: http://multivu.prnewswire.com/mnr/prne/sanofi/48930/