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Metastatic Castrate-Resistant Prostate Cancer Subjects Treated With PROVENGE® + One Infusion of Sipuleucel-T
NCT06134232 · View on ClinicalTrials.gov ↗
Study Summary
A multicenter, open-label, prospective study to investigate immune boost response changes in patients with metastatic castrate-resistant prostate cancer (mCRPC).
Conditions Studied
Interventions
- DRUG Sipuleucel-T Injection
Study Locations (20)
Florida
- Advanced Urology Institute — Daytona Beach
- Advanced Urology Institute — Largo
- Advanced Urology Institute — Ocala
- Florida Urology Partners — Riverview
California
- City of Hope - National Medical Center — Duarte
- Urology Associates of Central California Medical Group — Fresno
- Unio Health Partners - Genesis Research, LLC — San Diego
Illinois
- Associated Urological Specialists — Chicago Ridge
- UroPartners — Glenview
- Advanced Urology Associates — New Lenox
Indiana
- Urology of Indiana — Carmel
- First Urology — Jeffersonville
- Urologic Specialists of Northwest Indiana — Merrillville
New York
- Integrated Medical Professionals — North Hills
- Associated Medical Professionals of NY — Syracuse
Arizona
- Arizona Urology Specialists — Tuscon
Colorado
- Colorado Urology — Lakewood
Maryland
- Chesapeake Urology Research Associates — Towson
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 400 participants |
| Start Date | 2023-10-02 |
| Est. Completion | 2032-06-30 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06134232
The ClinicalTrials.gov registry entry for NCT06134232 describes a study currently listed as recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 400 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Dendreon, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Metastatic Castration-Resistant Prostate Cancer (mCRPC) appearing as the primary indexed condition, and to 1 intervention — of which Sipuleucel-T Injection is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06134232 reports 20 study locations spanning 10 distinct geographic areas — top geographies include Florida, California, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06134232 about?
NCT06134232 is a clinical study titled "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).
What is the current status of trial NCT06134232?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 400 participants. The study started on 2023-10-02. Estimated completion is 2032-06-30.
What conditions does trial NCT06134232 study?
This clinical trial studies the following conditions: Metastatic Castration-Resistant Prostate Cancer (mCRPC). These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06134232?
The interventions under investigation include: Sipuleucel-T Injection (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06134232?
This trial is sponsored by Dendreon, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06134232 being conducted?
This trial has 20 study locations across Arizona, California, Colorado, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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