FDA Approves Provenge for Advanced Prostate Cancer

Dendreon Corp. received approval from the FDA for Provenge (sipuleucel-T), an autologous cellular immunotherapy for the treatment of asymptomatic or minimally symptomatic metastatic, castrate-resistant (hormone-refractory) prostate cancer (CRPC).

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By: Tim Wright

Editor-in-Chief, Contract Pharma

Dendreon Corp. received approval from the FDA for Provenge (sipuleucel-T), an autologous cellular immunotherapy for the treatment of asymptomatic or minimally symptomatic metastatic, castrate-resistant (hormone-refractory) prostate cancer (CRPC). Provenge is designed to induce an immune response against prostatic acid phosphatase (PAP), an antigen expressed in most prostate cancers. “The FDA approval of Provenge is a testament to the courage of the patients and researchers who participa...

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