Healthcare Industry News: Aranesp
News Release - September 7, 2006
Amgen Launches Aranesp(R) (Darbepoetin Alfa) Prefilled SureClick(TM) Autoinjector for Treatment of Anemia Associated with Chemotherapy and Chronic Kidney DiseaseNew Autoinjector Offers Secure and Simple Way to Administer Anemia Treatment
THOUSAND OAKS, Calif.--(HSMN NewsFeed)--Sept. 7, 2006--Amgen (NASDAQ:AMGN ) today announced the launch of the Aranesp® (darbepoetin alfa) prefilled SureClick(TM) autoinjector for patients with chemotherapy-induced anemia and anemia associated with chronic kidney disease (CKD) in the United States.
"With the availability of the Aranesp prefilled SureClick autoinjector, healthcare providers and patients now have a new secure and simple option that automatically delivers a complete subcutaneous injection in a single use," said Willard Dere, M.D., senior vice president for Global Development and chief medical officer at Amgen. "The added safety features of the SureClick autoinjector minimize potential needlestick injuries, offering dependable benefits for nurses, oncologists and nephrologists who administer Aranesp in clinics and hospitals."
The Aranesp prefilled SureClick autoinjector has three important and unique safety features, including a safety cover that limits needle exposure before and after the subcutaneous injection, two audible clicks to announce the beginning and end of the injection, and a large inspection window that confirms it automatically delivered the complete injection. In a survey that included the use of the Aranesp prefilled SureClick autoinjector, most oncology nurses agreed that the device was easy to use.
The Centers for Disease Control and Prevention (CDC) estimates that one out of every seven healthcare professionals is accidentally stuck by a contaminated sharp, most often a needle, each year. Approximately 62 to 88 percent of needlestick injuries can potentially be prevented by the use of safer devices. To reduce these occupational hazards, the CDC has identified eight desirable characteristics for safety devices, and the Aranesp prefilled SureClick autoinjector has at least six of these characteristics.
The FDA approval of the Aranesp prefilled SureClick autoinjector broadens current administration options for healthcare providers and patients with anemia associated with chemotherapy and CKD. There are now three administration options for Aranesp: single-use SureClick autoinjector, SingleJect® prefilled syringes and prefilled vials. This wide range of delivery options allows healthcare professionals to select the option that best meets their needs and their patients' and staffs' needs. The Aranesp prefilled SureClick autoinjector will be available in clinics, hospitals and retail pharmacies, along with the other currently available administration options. Additionally, the Aranesp prefilled SureClick autoinjector will be offered at the same price as the other administration methods.
The Aranesp prefilled SureClick autoinjector, which was approved in the European Union in 2005 for patients with chemotherapy-induced anemia and anemia associated with CKD, has been delivered to approximately 500,000 patients to date.
About Chemotherapy-Induced Anemia
Chemotherapy can reduce the bone marrow's ability to produce red blood cells that transport oxygen from the lungs to all of the body's muscles and organs. Anemia occurs when there are too few red blood cells and the body's tissues are "starved" of oxygen, which can make a patient feel short of breath, very weak, faint and tired.
This year, an estimated 1.3 million cancer patients will undergo chemotherapy in the United States; approximately 800,000 (67 percent) will become anemic. More than half of chemotherapy patients report that fatigue, a common symptom of anemia, affects their daily lives more than any other side effect of treatment, including nausea, pain and depression.
Although anemia is one of the most common side effects of chemotherapy, it is often not recognized and frequently under-treated, despite treatments that have been available for more than a decade. In fact, approximately half of patients with a hemoglobin level less than the recommended target level of 11 to 12 g/dL in the National Comprehensive Cancer Network® (NCCN) guidelines for "Cancer and Treatment-Related Anemia" are never treated with erythropoietic therapy.
About Anemia and Chronic Kidney Disease (CKD)
According to the National Kidney Foundation, CKD affects 20 million Americans (one in nine adults) and more than 20 million others are at increased risk for developing kidney disease. CKD is an irreversible condition characterized by kidney damage and impaired function that often progresses over time. Patients with CKD often suffer from serious complications such as anemia, which occurs when failing kidneys no longer produce sufficient erythropoietin, a hormone that stimulates the production of oxygen-carrying red blood cells. Red blood cells contain hemoglobin, a red, iron-rich protein that carries oxygen from the lungs to all of the body's tissues. Oxygen provides the energy the body needs for normal activities. Anemia occurs when the number of red blood cells (or the hemoglobin in them) falls below normal (12 to 18 g/dL of blood). Therefore, the body gets less oxygen and does not have enough energy to function properly.
Amgen revolutionized anemia treatment with the development of Epoetin alfa, a recombinant erythropoietin (a protein that stimulates the production of oxygen-carrying red blood cells). Building on this heritage, Amgen developed Aranesp, a unique erythropoiesis-stimulating protein that can be dosed less frequently.
Aranesp was approved by the U.S. Food and Drug Administration (FDA) in September 2001 for the treatment of anemia associated with chronic renal failure (CRF), also known as CKD, for patients on dialysis and patients not on dialysis. In 2002, Aranesp was approved for the treatment of chemotherapy-induced anemia in patients with nonmyeloid malignancies in the U.S. and European Union (EU). Today, Aranesp is the only erythropoiesis-stimulating protein approved in the U.S. and EU for weekly and every-three-week administration, which allows physicians to synchronize anemia treatment with the majority of chemotherapy schedules. Since its introduction in 2001, more than 1.7 million CKD and chemotherapy patients with anemia have received treatment with Aranesp.
Important Safety Information
Aranesp is contraindicated in patients with uncontrolled hypertension. Erythropoietic therapies may increase the risk of thrombotic events and other serious events. Seizures have occurred in patients with Chronic Kidney Disease. The target hemoglobin (Hb) should not exceed 12 g/dL. If the Hb increase exceeds 1.0 g/dL in any 2-week period, dose reductions are recommended. In a study of Epoetin alfa treated hemodialysis patients with clinically evident cardiac disease, where the target hematocrit (Hct) was 42 percent (Hb = 14 g/dL), an increased incidence of thrombotic events and mortality was seen. The reason for increased mortality observed in this study is unknown. In a study with another erythropoietic product, in women with metastatic breast cancer receiving chemotherapy, where the target Hb was 12-14 g/dL, an increased incidence of thrombotic events, disease progression, and mortality was seen.
Cases of pure red cell aplasia (PRCA) and of severe anemia, with or without other cytopenias associated with neutralizing antibodies to erythropoietin have been reported in patients treated with Aranesp. This has been reported predominately in patients with CRF receiving Aranesp by subcutaneous administration. A sudden loss of response to Aranesp, accompanied by severe anemia and low reticulocyte count, should be evaluated. If anti-erythropoietin antibody-associated anemia is suspected, withhold Aranesp and other erythropoietic proteins. Aranesp should be permanently discontinued in patients with antibody-mediated anemia. Patients should not be switched to other erythropoietic proteins.
The most commonly reported side effects in clinical trials in patients with CRF were infection, hypertension, hypotension, myalgia, headache, and diarrhea. The most commonly reported side effects in clinical trials in patients with chemotherapy-induced anemia were fatigue, edema, nausea, vomiting, diarrhea, fever, and dyspnea.
Amgen discovers, develops and delivers innovative human therapeutics. A biotechnology pioneer since 1980, Amgen was one of the first companies to realize the new science's promise by bringing safe and effective medicines from lab, to manufacturing plant, to patient. Amgen therapeutics have changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, and other serious illnesses. With a broad and deep pipeline of potential new medicines, Amgen remains committed to advancing science to dramatically improve people's lives. To learn more about our pioneering science and our vital medicines, visit www.amgen.com.
This news release contains forward-looking statements that involve significant risks and uncertainties, including those discussed below and others that can be found in Amgen's Form 10-K for the year ended December 31, 2005, and in Amgen's periodic reports on Form 10-Q and Form 8-K. Amgen is providing this information as of the date of this news release and does not undertake any obligation to update any forward-looking statements contained in this document as a result of new information, future events or otherwise.
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The scientific information discussed in this news release related to our product candidates is preliminary and investigative. Such product candidates are not approved by the U.S. Food and Drug Administration (FDA), and no conclusions can or should be drawn regarding the safety or effectiveness of the product candidates. Only the FDA can determine whether the product candidates are safe and effective for the use(s) being investigated. Further, the scientific information discussed in this news release relating to new indications for our products is preliminary and investigative and is not part of the labeling approved by the FDA for the products. The products are not approved for the investigational use(s) discussed in this news release, and no conclusions can or should be drawn regarding the safety or effectiveness of the products for these uses. Only the FDA can determine whether the products are safe and effective for these uses. Healthcare professionals should refer to and rely upon the FDA-approved labeling for the products, and not the information discussed in this news release.
Aranesp prescribing information can be accessed by calling 800-772-6436 or by logging on to www.Aranesp.com.
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