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NCT06134232
Metastatic Castrate-Resistant Prostate Cancer Subjects Treated With PROVENGE® + One Infusion of Sipuleucel-T
A multicenter, open-label, prospective study to investigate immune boost response changes in patients with metastatic castrate-resistant prostate cancer (mCRPC).
Trial Details
NCT ID NCT06134232
Phase PHASE2
Sponsor Dendreon
Status RECRUITING
Cancer Type Prostate Cancer
Interventions
Locations (sample) Tuscon, Arizona, United States Duarte, California, United States|34.13945,-117.97729 Fresno, California, United States|36.74773,-119.77237 San Diego, California, United States|32.71571,-117.16472 Lakewood, Colorado, United States|39.70471,-105.08137
Key Eligibility Criteria
For a subject to be eligible for participation in this study, all of the following criteria must be satisfied: Potential subjects are men aged ≥18 years who are clinically indicated for treatment with PROVENGE® (asymptomatic or minimally symptomatic metastat… Have qualified for on-label PROVENGE® infusion Have received all 3 infusions of PROVENGE® prior to randomization
For full eligibility, visit ClinicalTrials.gov .
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