Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Laguna Hills, California 92653


Purpose:

This study is being conducted to examine the immune response generated by sipuleucel-T in subjects previously treated with sipuleucel-T in the androgen dependent setting. The study will also assess the safety of receiving up to 3 additional infusions of sipuleucel-T. This is an open-label, uncontrolled, multicenter study, conducted in up to 14 clinical trial sites. The anticipated duration of the study is approximately 6 years.


Criteria:

Inclusion Criteria: - Previously randomized in Dendreon's P-11 study (NCT00779402) and received at least one infusion of sipuleucel-T - Radiologic evidence of metastasis - Castrate resistant prostate cancer. Subjects must have current or historical evidence of disease progression concomitant with surgical or medical castration, as demonstrated by PSA progression OR progression of measurable disease OR progression of non-measurable disease - Castrate level of testosterone (< 50 ng/dL) achieved via medical or surgical castration - Adequate hematologic function Exclusion Criteria: - Eastern Cooperative Oncology Group (ECOG) performance status > 2 - Treatment with chemotherapy within 3 months prior to registration - Treatment with systemic corticosteroids, external beam radiation therapy, or any investigational product for prostate cancer within 28 days prior to registration - Current or imminent pathologic long-bone fracture - Known malignancies other than prostate cancer that are likely to require treatment within 6 months following registration - A requirement for systemic immunosuppressive therapy for any reason - A history of allergic reactions attributed to compounds of similar chemical or biologic composition to sipuleucel-T or GM-CSF - Any infection requiring antibiotic therapy or causing fever within 1 week prior to registration - Any surgery requiring general anesthetic within 28 days prior to registration


NCT ID:

NCT01338012


Primary Contact:

Study Director
Robert Israel, MD
Valeant Pharmaceuticals North America LLC


Backup Contact:

N/A


Location Contact:

Laguna Hills, California 92653
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.