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Clinical Trial 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.


Clinical Trial Description

In 2011, more than 200,000 men in North America alone were diagnosed with cancer of the prostate, which makes it one of the most common cancer types. It affects the lives of the subjects in many ways. After treatment the subjects PSA levels are being closely monitored to detect potential recurrence. A high number of subjects will get recurrent prostate cancer. The treatment options for recurrent cancer are more limited than for primary tumors as secondary treatment partly depends on which treatment the subject has previously undergone. Treatment of recurrent prostate cancer may, depending on the standard treatment of the primary disease, include the following: - Radiation therapy. - Prostatectomy for subjects initially treated with radiation therapy. - Hormone therapy. - Pain medication, external radiation therapy, internal radiation therapy with radioisotopes such as strontium-89, or other treatments as palliative therapy to lessen bone pain. The objectives of this study is to demonstrate that the use of the SpectraCure P18 System (Interstitial multiple diode lasers and IDOSE® Software) and verteporfin for injection (VFI) is a safe treatment for recurrent prostate cancer. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03067051
Study type Interventional
Source SpectraCure AB
Contact Johannes Swartling
Phone +46 (0) 46 16 20 70
Email jsw@spectracure.com
Status Recruiting
Phase Phase 1/Phase 2
Start date March 21, 2017
Completion date December 31, 2024

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