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Study of WST09 in Prostate Cancer After Radiation: Repeat Procedure

Primary Purpose

Prostate Cancer

Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Treatment with Tookad VTP
Treatment with Tookad VTP
Treatment with Tookad VTP
Sponsored by
STEBA France
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring Treatment of localized prostate cancer, Localized prostate cancer

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria: Patients previously treated with WST09-mediated VTP, with a positive biopsy of the prostate 6 months following treatment Disease confined to the prostate Life expectancy greater than 5 years Exclusion Criteria: Unwilling or unable to give informed consent Patients who have received another treatment for their prostate cancer since their previous WST09-mediated VTP

Sites / Locations

  • The Prostate Centre Princess Margaret Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1

Arm Description

Treatment with Tookad VTP

Outcomes

Primary Outcome Measures

Prostate biopsy

Secondary Outcome Measures

MRI, PSA

Full Information

First Posted
March 20, 2006
Last Updated
May 31, 2010
Sponsor
STEBA France
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1. Study Identification

Unique Protocol Identification Number
NCT00305929
Brief Title
Study of WST09 in Prostate Cancer After Radiation: Repeat Procedure
Official Title
Phase II Study of Photodynamic Therapy With WST09 in Patients With Recurrent or Persistent Localized Carcinoma of the Prostate Following Radiation Therapy Failure - Repeat Procedure
Study Type
Interventional

2. Study Status

Record Verification Date
May 2010
Overall Recruitment Status
Completed
Study Start Date
March 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
STEBA France

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a multi-centre, phase II, open-label, 12-month clinical trial for patients previously treated with WST09 (Tookad) who have positive prostate biopsies for cancer. The study aims at delivering a second WST09 treatment for the purpose of eradicating the localized prostate cancer.
Detailed Description
Multi-centre, phase II, open-label, 12-month clinical trial for patients that previously received a vascular-targeted photodynamic treatment (VTP) with WST09 (Tookad) and still have histological findings (prostate biopsies) indicating the presence of localized cancer. The WST09-mediated VTP procedure consists of an I.V. infusion of WST09 (Tookad) at 2 mg/kg, in combination with the per-cutaneous interstitial delivery of monochromatic laser light (of a wavelength of 763nm) via the trans-perineal implantation of illumination fibres, positioned in the prostatic lobes. In a previous Tookad trial, escalating doses of laser light were used with a fixed dose of WST09 (2 mg/kg) in patients with localized prostatic cancer. Patients who underwent the procedure but still have positive prostate biopsies (residual cancer) may benefit from an additional WTS09-mediated VTP procedure. Thus, the aim of this study is to treat patients still presenting with localized prostate cancer with a second WST09-mediated VTP procedure.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Treatment of localized prostate cancer, Localized prostate cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
8 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Treatment with Tookad VTP
Intervention Type
Drug
Intervention Name(s)
Treatment with Tookad VTP
Other Intervention Name(s)
WST09
Intervention Type
Drug
Intervention Name(s)
Treatment with Tookad VTP
Intervention Description
Tookad 2 mg/kg
Intervention Type
Drug
Intervention Name(s)
Treatment with Tookad VTP
Intervention Description
2 mg/kg
Primary Outcome Measure Information:
Title
Prostate biopsy
Time Frame
12 months
Secondary Outcome Measure Information:
Title
MRI, PSA
Time Frame
7 days, 6 months

10. Eligibility

Sex
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients previously treated with WST09-mediated VTP, with a positive biopsy of the prostate 6 months following treatment Disease confined to the prostate Life expectancy greater than 5 years Exclusion Criteria: Unwilling or unable to give informed consent Patients who have received another treatment for their prostate cancer since their previous WST09-mediated VTP
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John Trachtenberg, MD, FRCS(C)
Organizational Affiliation
University Health Network, Princess Margaret Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Prostate Centre Princess Margaret Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2M9
Country
Canada

12. IPD Sharing Statement

Learn more about this trial

Study of WST09 in Prostate Cancer After Radiation: Repeat Procedure

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