Advertisement Alkermes Vivitrol gets FDA nod - Pharmaceutical Business review
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Alkermes Vivitrol gets FDA nod

Alkermes' Vivitrol (naltrexone for extended-release injectable suspension), used for the prevention of relapse to opioid dependence, following opioid detoxification, has received approval from the US Food and Drug Administration (FDA).

Alkermes claimed that Vivitrol is a non-narcotic, non-addictive, once-monthly medication approved for the treatment of opioid dependence.

The FDA approval of Vivitrol for the prevention of relapse to opioid dependence was based on data from a six-month, multi-center, randomised Phase 3 study which met its primary efficacy endpoint and all secondary efficacy endpoints.

In 2006, Vivitrol received approval for the treatment of alcohol dependence and should be used as part of a comprehensive management program that includes psychosocial support.

Alkermes CEO Richard Pops said that they believe that Vivitrol offers physicians and their patients a whole new approach, as the only long-acting, non-addictive treatment for opioid dependence.