Bridgewater, N.J. – August 12, 2014 / PR Newswire / — Sanofi US announced today that it has launched an authorized generic version of Eloxatin® (oxaliplatin injection) through Winthrop US, the company’s generics division. Sanofi’s authorized generic version is the same formulation as the original drug, Eloxatin, for which the company holds the original patent.
Eloxatin is a platinum–based drug used in combination with infusional 5–fluorouracil/leucovorin. This treatment is indicated for treatment of advanced colorectal cancer or as adjuvant treatment of stage III colon cancer in patients who have undergone complete resection of the primary tumor. The authorized generic version of Eloxatin will be available in the same sizes, 50 mg and 100 mg single–use vials.
“We are committed to broadening access to our medicines and providing more affordable treatment options for patients,” said Charles Hugh-Jones, MD, FRCP, Chief Medical Officer, North America, Sanofi. “The availability of an authorized generic version of Eloxatin is welcomed news for patients and physicians alike.”
According to the Centers for Disease Control and Prevention (CDC), “of cancers that affect both men and women, colorectal cancer is the second leading cancer killer in the United States.”1
Winthrop US delivers affordable solutions to the healthcare community by transforming Sanofi’s branded products into authorized generics and is devoted to supplying high quality products to its customers with excellent service.
Important Safety Information for Eloxatin® (oxaliplatin injection)
ELOXATIN can cause serious allergic reactions, including allergic reactions that may cause death. ELOXATIN is a platinum–based medicine. Serious allergic reactions including death can occur in people who take ELOXATIN and who have had previous allergic reactions to platinum medicines. Serious allergic reaction can happen within a few minutes of your infusion or any time during your treatment with ELOXATIN.
Tell your doctor if you have any side effect that bothers you or that does not go away. These are not all the possible side effects of ELOXATIN. For more information, ask your doctor or pharmacist.
Please click here for full Prescribing Information for Eloxatin® (oxaliplatin injection), including Boxed WARNING, and visit: http://products.sanofi.us/eloxatin/eloxatin.html
Sanofi, a global 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, consumer healthcare, emerging markets, animal health and the new Genzyme. Sanofi is listed in Paris (EURONEXT: SAN) and in New York (NYSE: SNY).
Forward Looking Statements
This press release contains forward–looking statements as defined in the Private Securities Litigation Reform Act of 1995, as amended. Forward–looking statements are statements that are not historical facts. These statements include projections and estimates and their underlying assumptions, statements regarding plans, objectives, intentions and expectations with respect to future financial results, events, operations, services, product development and potential, and statements regarding future performance. Forward–looking statements are generally identified by the words “expects”, “anticipates”, “believes”, “intends”, “estimates”, “plans” and similar expressions. Although Sanofi’s management believes that the expectations reflected in such forward–looking statements are reasonable, investors are cautioned that forward–looking information and statements are subject to various risks and uncertainties, many of which are difficult to predict and generally beyond the control of Sanofi, that could cause actual results and developments to differ materially from those expressed in, or implied or projected by, the forward–looking information and statements. These risks and uncertainties include among other things, the uncertainties inherent in research and development, future clinical data and analysis, including post marketing, decisions by regulatory authorities, such as the FDA or the EMA, regarding whether and when to approve any drug, device or biological application that may be filed for any such product candidates as well as their decisions regarding labelling and other matters that could affect the availability or commercial potential of such product candidates, the absence of guarantee that the product candidates if approved will be commercially successful, the future approval and commercial success of therapeutic alternatives, the Group’s ability to benefit from external growth opportunities, trends in exchange rates and prevailing interest rates, the impact of cost containment policies and subsequent changes thereto, the average number of shares outstanding as well as those discussed or identified in the public filings with the SEC and the AMF made by Sanofi, including those listed under “Risk Factors” and “Cautionary Statement Regarding Forward–Looking Statements” in Sanofi’s annual report on Form 20–F for the year ended December 31, 2013. Other than as required by applicable law, Sanofi does not undertake any obligation to update or revise any forward–looking information or statements.
1Centers for Disease Control and Prevention. Basic information about colorectal cancer. Available at: http://www.cdc.gov/cancer/colorectal/basic_info/. Accessed July 28, 2014.