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Dendreon Announces Presentation Of PROVENGE® (sipuleucel-T) And DN24-02 Immuno-Oncology Data At The 2014 ASCO Annual Meeting

May 14, 2014 – Dendreon Corporation (NASDAQ: DNDN) announced today the presentation of two PROVENGE ® (sipuleucel-T) abstracts from the Phase II STAND study and the PROCEED registry, and one abstract highlighting data from the ongoing Phase II study of DN24-02, an investigational active cellular immunotherapy for patients with surgically resected HER2+ urothelial cancer. These data will be presented at the 50 th Annual Meeting of the American Society of Clinical Oncology (ASCO) from May 30-June 3, 2014 in Chicago, Illinois.

Additionally, preliminary data from the Phase II STRIDE study evaluating concurrent or sequential treatment of PROVENGE with enzalutamide are available online at

“These data continue to help reinforce how PROVENGE may be combined or sequenced with other advanced prostate cancer treatments,” said Andrew S. Sandler, M.D., executive vice president and chief medical officer at Dendreon. “We remain committed to our active cellular immunotherapy platform and expanding the medical community’s understanding of how immuno-oncology treatments can be used to benefit patients.”

Dendreon will present the following studies evaluating PROVENGE and DN24-02 data at ASCO:
  • A Randomized Phase II Study Evaluating the Optimal Sequencing of Sipuleucel-T and Androgen Deprivation Therapy (ADT) in Biochemically-Recurrent Prostate Cancer (BRPC): Preliminary Clinical Data. Data from the Phase II STAND study suggest cytokine responses may be superior when PROVENGE is given after the start of treatment with ADT (rather than before) to patients with biochemically-recurrent prostate cancer. General Poster Session: Monday, June 2, 1:15 PM – 5:00 PM CT, S Hall A2, Poster Board #170
  • Time to Chemotherapy Following Treatment with Sipuleucel-T: Data from PROCEED. An analysis of data from the PROCEED registry suggests that younger age, lower hemoglobin or higher PSA at baseline prior to PROVENGE therapy is associated with shorter time to chemotherapy after PROVENGE. General Poster Session: Monday, June 2, 1:15 PM – 5:00 PM CT, S Hall A2, Poster Board #169
  • Preliminary Product Parameter and Safety Results from NeuACT, a Phase II Randomized, Open-Label Trial of DN24-02 in Patients with Surgically Resected HER2+ Urothelial Cancer at High Risk for Recurrence. A preliminary analysis of data from the randomized Phase II NeuACT study suggests DN24-02, targeted towards the HER2 antigen, has a similar immune effect as PROVENGE in the activation of antigen presenting cells and heightened T-cell cytokines consistent with immunological prime-boost response. General Poster Session: Monday, June 2, 1:15 PM – 5:00 PM CT, S Hall A2, Poster Board #109

“These data support the current clinician perception that the future of cancer treatments should be a personalized approach, including immunotherapies,” said Daniel Petrylak, M.D., professor of medicine, director of Genitourinary Oncology, co-director of Signal Transduction Research Program, Yale Cancer Center and Smilow Cancer Hospital at Yale-New Haven. “We continue to see powerful evidence of meaningful immunological responses to immunotherapies such as sipuleucel-T and investigational compound DN24-02.”

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