Status:
COMPLETED
Safety and Tolerability Study Using WST11 In Patients With Localized Prostate Cancer
Lead Sponsor:
Steba Biotech S.A.
Conditions:
Prostate Cancer
Eligibility:
MALE
18+ years
Phase:
PHASE1
PHASE2
Brief Summary
The aim of this study is to determine the optimal treatment conditions (WST11 dose and light energy dose) to achieve ablation in one lobe of the prostate and to evaluate the safety and quality of life...
Detailed Description
This study is designed as a multicenter, phase I/II, prospective, open-labeled, single intravenous (IV) dose, clinical trial in patients with localized prostate cancer. The study population will be m...
Eligibility Criteria
Inclusion
- At least 18 years of age
- Diagnosed with localized, prostate cancer and who have been offered curative therapy (radical prostatectomy; cryotherapy; brachytherapy; External Beam RadioTherapy (EBRT), and refused
- Localized prostate cancer stage T1C up to T2A based on biopsy performed at least 6 weeks prior to enrollment
- Gleason score ≤ 3+3 with ≤50% of sampled cores positive, and each positive core having a tumour length of ≤5 mm
- Prostate Specific Antigen (PSA) \< 10 ng/mL
- No prior treatment for prostate cancer
- Signed Informed Consent Form
Exclusion
- Any condition or history of illness or surgery that, in the opinion of the investigator and/or the Sponsor, might confound the results of the study or pose additional risks to the patient.
- All patients whose current pre-operative cardiac evaluation does not show their fitness for a procedure requiring general anesthesia;
- Patients with a prior history of viral or alcoholic hepatitis, and other patients felt to be at risk for hepatotoxicity including concomitant use of potentially hepatotoxic medications or dietary supplements;
- Patients with a history of inflammatory bowel disease or other factors which may increase the risk of fistula formation;
- Patients who have received any hormonal manipulation (excluding 5-alpha reductase inhibitors) or androgen supplements within the previous 6 months;
- Patients previously treated by radiation therapy (external therapy or brachytherapy) or chemotherapy or any therapy for prostate cancer;
- Patients who have received or are receiving chemotherapy for prostate carcinoma or other significant cancer;
- Patients who have undergone previous TURP (trans-urethral resection of the prostate);
- Patients with a history of urethral stricture disease
- Patients with a history of acute urinary retention
- Patients who are currently (within 10 days before the treatment procedure) receiving any medications having potential photosensitizing effects (e.g. tetracyclines, sulfonamides, phenothiazines, sulfonylurea hypoglycemic agents, thiazide diuretics and griseofulvin)
- Patients who are currently receiving anticoagulant drugs (within 10 days before the treatment procedure) (e.g.: coumadin, warfarin)
- Patient who stopped long term treatment of acetylsalicylic acid (aspirin) or other anti platelets agents within 10 days prior to the treatment procedure;
- Patient suspected of Disseminated Intravascular Coagulation (DIC) as defined by the presence of three out of the five following criteria: platelets decrease, increase of PT, increase of aPTT, fibrinogen decrease, D-Dimer increase; from the normal laboratory ranges;
- Patient with a history of vasculitis or collagen vascular disease;
- History of non compliance with medical therapy and medical recommendations or an unwillingness or inability to complete patient self-administered questionnaires;
- Participation in a clinical study or receipt of an investigational treatment within the past 3 months;
- A history of porphyria;
- A history of sun hypersensitivity or photosensitive dermatitis;
- Renal disorders (blood creatinine \> 1.5 x ULN) or known post mictional residue \> 150cc
- Hepatic disorders (transaminases \> ULN, bilirubin \> ULN, GGT \> ULN). In case of slight abnormalities, another exam could be performed. If the results are within normal ranges, then the patient can be included;
- Hematological disorders (white cells \< 2500/mm3, neutrophils \< 1500/mm3, platelets, \< 140.000/mm3, Hb ≤ 10 g/dL);
- Patients with contra-indication to MRI (such as pace maker, metal prosthesis, etc.).
Key Trial Info
Start Date :
July 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2012
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT00946881
Start Date
July 1 2009
End Date
August 1 2012
Last Update
February 7 2024
Active Locations (5)
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1
UCLA - Jonsson Comprehensive Cancer Center
Los Angeles, California, United States, 90095
2
Midtown Urology & Midtown Urology Surgical Center
Atlanta, Georgia, United States, 30308
3
Washington University School of Medicine- Barnes-Jewish Hospital
St Louis, Missouri, United States, 63110
4
NYU Urology Associates
New York, New York, United States, 10016