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| | | ![]() Vivitrol, the First, Once-Monthly Injectable Medication for Alcohol Dependence Now Available in the United States FRAZER, PA, and CAMBRIDGE, MA -- June 13, 2006 -- Cephalon, Inc. and Alkermes, Inc. today announced that Vivitrol(TM) (naltrexone for extended-release injectable suspension), the first and only once-monthly injectable medication for alcohol dependence, is now commercially available in the United States. Vivitrol is indicated for patients who are able to abstain from drinking in an outpatient setting and are not actively drinking when initiating treatment. Vivitrol should be used as part of a comprehensive treatment management program, which includes psychosocial support, such as counseling or group therapy. The U.S. Food and Drug Administration (FDA) approved Vivitrol in April 2006. In clinical studies, those treated with Vivitrol demonstrated a greater reduction in the number of heavy drinking days than those treated with placebo. In a subset of patients who abstained from drinking in the week prior to receiving their first dose of medication, those treated with Vivitrol 380 mg were more likely to maintain complete abstinence (without relapse) and showed a greater reduction in heavy drinking, as well as a greater reduction in heavy drinking days, compared to the placebo-treated group over the six- month treatment period. Vivitrol is administered by a healthcare provider. Frequent interactions with healthcare providers could strengthen the therapeutic alliance - the collaborative relationship a healthcare professional is able to form with a patient - a crucial factor in the success of therapy. Vivitrol also provides patients with the convenience of monthly dosing, which alleviates the need for patients to remember to take a daily oral medication. VIP3: Unique Program to Support the Treatment of Alcohol Dependence with Vivitrol Vivitrol is available through a limited network of specialty pharmacy providers, including Coram, Inc., Caremark, PharmaCare Specialty Pharmacy, Aetna Specialty Pharmacy and CuraScript. These pharmacies have specialized capabilities to meet the storage and handling needs of Vivitrol and will be working through the VIP3 program to coordinate product distribution. "With more than 400 physicians currently enrolled in VIP3, our professional education plans, and a combined field presence of Cephalon and Alkermes personnel, we are confident Vivitrol will be a success and that many patients will benefit from this important new therapy," stated Robert P. Roche, Jr., Executive Vice President, Worldwide Pharmaceutical Operations at Cephalon. Vivitrol combined with psychosocial support and the VIP3 support program may help patients with alcohol dependence stay on the road to recovery. "With Vivitrol and my counseling sessions, I was able to stay sober and focus on other important things in my life," said Laurie O'Connor, a person in recovery from alcohol dependence and Vivitrol clinical trial participant. "I am just the average woman. If I can have a problem with alcoholism, I know other people can too. I would just like to reach out to those people and their families to tell them that more help is available." About Vivitrol The proprietary Medisorb(R) drug delivery technology in Vivitrol enables the medication to be gradually released into the body at a controlled rate over a one-month time period. Vivitrol works by binding to opioid receptors in the brain. Although the mechanism responsible for the reduction in alcohol consumption observed with Vivitrol treatment is not entirely understood, preclinical data suggests that occupation of the opioid receptors results in the blockade of the neurotransmitters in the brain that are believed to be involved with alcohol dependence. This blockade may result in the reduction in alcohol consumption observed in patients treated with Vivitrol. Important Safety Information WARNING Vivitrol is contraindicated in patients receiving opioid analgesics, with current physiologic dependence on opioids, in acute opioid withdrawal or who have previously exhibited hypersensitivity to naltrexone, PLG or any other components of the diluent. Vivitrol is a potent opioid antagonist. Patients must be opioid free for a minimum of seven to 10 days before starting Vivitrol treatment. Any attempt to overcome the opioid blockade produced by Vivitrol using exogenous opioids may result in fatal overdose. In patients with a previous history of opioid abuse, administration of exogenous opioids may result in potentially life- threatening opioid intoxication. When reversal of Vivitrol blockade is required for pain management, patients should be monitored in a setting equipped and staffed for cardiopulmonary resuscitation. Should a patient receiving Vivitrol develop progressive dyspnea and hypoxemia, the diagnosis of eosinophilic pneumonia should be considered. Patients should be advised to seek medical attention for injection site reactions such as pain, tenderness, induration or pruritus that do not improve within one month following the injection. Alcohol dependent patients, including those taking Vivitrol, should be monitored for the development of depression or suicidal thinking. About Alcohol Dependence Of the more than 18 million Americans who abuse or are dependent on alcohol,(3) approximately 2.2 million seek treatment for their alcohol problems.(4) More than 75% of these patients relapse back to drinking within the first year of beginning treatment using currently available treatment approaches.(5) Alcohol abuse and dependency are an economic burden to society that costs approximately $185 billion annually in the U.S.(6)
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SOURCE: Cephalon, Inc.; Alkermes, Inc.
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