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nvidia vanta lt driver |
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nvidia vanta lt driver Generic Name: histrelin implant Date of Approval: October 12, 2004 Company: Valera Pharmaceuticals Treatment for: Prostate Cancer The U.S nvidia vanta lt driver. 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) nvidia vanta lt driver. LHRH agonists have become a mainstay in treating locally advanced and metastaticprostate cancer with the U.S nvidia vanta lt driver. market for such therapies representing over $1billion in annual sales nvidia vanta lt driver. 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 nvidia vanta lt driver. 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 nvidia vanta lt driver. 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 nvidia vanta lt driver. Thus, Valera expects theVantas implant to offer benefits that include less patient discomfort and improvedtherapeutic compliance. |
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