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Dendreon Reports First Quarter 2011 Financial Results
Date:5/2/2011

dditional workstations will come online in a staged approach.
  • Dendreon filed for FDA approval of the Los Angeles area manufacturing facility and has an action date of June 30, 2011. 
  • Dendreon filed for FDA approval of the Atlanta facility on April 28 and expects a decision in late August or early September.
  • The Centers for Medicare and Medicaid Services (CMS) issued a proposed decision memo supporting the on-label coverage of PROVENGE.
  • Dendreon selected a contract manufacturing organization in Europe and a location for a manufacturing facility outside Frankfurt, Germany.

  • "We are proud of our accomplishments as we continue to expand the launch of PROVENGE.  Our recent increased sales and marketing efforts have had an impact, and we will continue to build on this momentum as we bring additional capacity online throughout this year to make PROVENGE more broadly available," said Mitchell H. Gold, M.D., president and chief executive officer.

    Conference Call InformationDendreon will host a conference call on May 2, 2011 at 4:30 p.m. ET. To access the live call, dial 1-877-548-9590 (domestic) or +1-720-545-0037 (international); the conference ID number is 57436485. The call will also be audio webcast and will be available from the Company's website at http://www.dendreon.com under the "Investor/Webcasts and Presentations" section. A recorded rebroadcast will be available for interested parties unable to participate in the live conference call by dialing 1-800-642-1687 or +1-706-645-9291 for international callers; the conference ID number is 57436485. The replay will be available from 7:30 p.m. ET on May 2 until 11:59 p.m. ET on May 9. In addition, the webcast will be archived for on-demand listening for 30 days at http://www.dendreon.com.

    About DendreonDendreon Corporation is a biotechnology company whose mission is to
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