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Clinical Study to Assess the Safety and Efficacy of the SpectraCure P18 System
NCT03067051 · View on ClinicalTrials.gov ↗
Study Summary
The rationale for the study is to obtain safety and efficacy data as well as to establish dose parameters for the SpectraCure P18 System with IDOSE®, with verteporfin for injection (VFI) as photosensitizer for the treatment of recurrent prostate cancer.
Conditions Studied
Interventions
- DRUG Verteporfin
- DEVICE SpectraCure P18 System
Study Locations (4)
New York
- Memorial Sloan Kettering Cancer Center — New York
Ontario
- Princess Margaret Cancer Centre — Toronto
Skåne County
- Skåne University Hospital — Malmo
Other
- Reader in Urology, University College London & Honorary Consultant Urological Surgeon, University College London Hospitals Trust — London
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 66 participants |
| Start Date | 2017-03-21 |
| Est. Completion | 2026-12-31 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03067051
The ClinicalTrials.gov registry entry for NCT03067051 describes a study currently listed as recruiting. It is categorized as Phase 1, 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 66 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is SpectraCure AB, which has 33 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 Recurrent Prostate Cancer appearing as the primary indexed condition, and to 2 interventions — of which Verteporfin 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: NCT03067051 reports 4 study locations spanning 4 distinct geographic areas — top geographies include New York, Ontario, Skåne County. 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 NCT03067051 about?
NCT03067051 is a clinical study titled "Clinical Study to Assess the Safety and Efficacy of the SpectraCure P18 System". The rationale for the study is to obtain safety and efficacy data as well as to establish dose parameters for the SpectraCure P18 System with IDOSE®, with verteporfin for injection (VFI) as photosensitizer for the treatment of recurrent prostate cancer.
What is the current status of trial NCT03067051?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 66 participants. The study started on 2017-03-21. Estimated completion is 2026-12-31.
What conditions does trial NCT03067051 study?
This clinical trial studies the following conditions: Recurrent Prostate Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03067051?
The interventions under investigation include: Verteporfin (DRUG), SpectraCure P18 System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03067051?
This trial is sponsored by SpectraCure AB, which has 33 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03067051 being conducted?
This trial has 4 study locations across New York, Ontario, Skåne County. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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