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tnt2 m64 vanta mx chip |
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tnt2 m64 vanta mx chip Generic Name: histrelin implant Date of Approval: October 12, 2004 Company: Valera Pharmaceuticals Treatment for: Prostate Cancer The U.S tnt2 m64 vanta mx chip. Food and Drug Administration (FDA) has approved the marketing of Vantas,a long-acting implant indicated for the palliative treatment of advanced prostatecancer. Utilizing Valera's Hydron Implant technology, Vantas has been designed for thecontinuous 12-month administration of histrelin, a synthetic nonapeptide agonistof luteinizing hormone-releasing hormone (LHRH) tnt2 m64 vanta mx chip. LHRH agonists have become a mainstay in treating locally advanced and metastaticprostate cancer with the U.S tnt2 m64 vanta mx chip. market for such therapies representing over $1billion in annual sales tnt2 m64 vanta mx chip. However, this market is dominated by 4-month and shorterduration depot injections or implants, led by Lupron Depot (leuprolide acetatefor depot suspension) from TAP Pharmaceutical Products Inc tnt2 m64 vanta mx chip. and includes Zoladex(goserelin acetate implant) from AstraZeneca PLC. Valera’s Hydron Implant technology utilizes proprietary blends of hydrogelpolymers, the same technology that originally led to the formulation of softcontact lenses tnt2 m64 vanta mx chip. In addition to providing for the administration of small, butpotent amounts of therapeutics at a controlled rate for up to a year or more,this technology platform allows for the formulation of highly compact, lightweight, flexible and retrievable subcutaneous implants that can be insertedin a physician’s office with a local anesthetic tnt2 m64 vanta mx chip. Thus, Valera expects theVantas implant to offer benefits that include less patient discomfort and improvedtherapeutic compliance. |
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