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Abbott Seeks FDA Approval of a New Six-Month 45-mg Formulation of Lupron(R) Depot for the Palliative Treatment of Advanced Prostate Cancer
Date:3/11/2010

About Lupron Depot

Lupron® Depot belongs to a class of medications known as gonadotropin releasing hormone agonists (GnRHa).  Lupron was first approved for subcutaneous injection in 1985 and was supported by results from clinical trials which demonstrated the efficacy and safety from daily injections.  Lupron Depot 7.5 mg was approved in 1989 followed by Lupron Depot three-month (22.5 mg) and Lupron Depot four-month (30 mg).  

Use

Lupron® Depot (leuprolide acetate for depot suspension) 7.5 mg, three-month 22.5 mg and four-month 30 mg are prescribed for the palliative treatment of advanced prostate cancer.


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