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Spots Global Cancer Trial Database for Study of WST11 in Patients With Localized Prostate Cancer

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Trial Identification

Brief Title: Study of WST11 in Patients With Localized Prostate Cancer

Official Title: Vascular-Targeted Photodynamic Therapy Using WST 11 in Patients With Localized Prostate Cancer

Study ID: NCT00707356

Conditions

Prostate Cancer

Interventions

WST11

Study Description

Brief Summary: The aim of this clinical study is to determine the optimal treatment conditions to achieve prostate cancer tumor ablation and to assess the effects of WST11 mediated VTP treatment in patients with localized prostate cancer. The secondary objectives is to evaluate safety and quality of life ; to assess the pharmacokinetic parameters and to model the relationship between concentration and effects; and to assess the effects, the safety and quality of life of a second WST11 VTP treatment in patients with persistent or recurrent localized prostate cancer after a first VTP;

Detailed Description: This trial is designed as a multicentre, phase II, open-labeled, single intra-venous (IV) dose study. The patient is to receive general anesthesia. WST11-mediated VTP will consist of the combination of a single IV administration of WST11 at doses of 2 mg/Kg,4mg/Kg or 6 mg/kg, using 753 nm laser light at a fixed power (150mW/cm) and energy (200 J/cm) delivered through transperineal interstitial optical fibers. If deemed necessary and in consideration of the results of the patients treated with 200 J/cm, alternate power (200mW/cm) and alternate energy (300 J/cm) might be applied after Sponsor, Steering Committee and DSMB approval.The fibers are introduced into transparent needles that are positioned in the prostate under ultra sound image guidance (using a brachytherapy like template). The tumor location is established using transrectal biopsy and MR imaging. The number of fibers and the total light energy will be adapted to each patient, taking into account the tumor localization and the volume of the prostate.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

University Health Network-Princess Margaret Hospital, Toronto, , Canada

Centre Hospitalier Universitaire, Angers, , France

Hôpital Bocage-CHU, Dijon, , France

Hôpital Claude Huriez, Lille, , France

Institut Mutualiste Montsouris(IMM), Paris, , France

Frimley Park Hospital NHS Trust, Frimley, , United Kingdom

Kings College Hospital(KCH), London, , United Kingdom

Urology Directorate, London, , United Kingdom

Contact Details

Name: Mark EMBERTON, Professor

Affiliation: Urology Directorate

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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