NCT Number: NCT01303991
Hexvix Photodynamic Therapy in Patients With Bladder Cancer
The purpose of the study is to investigate the safety and feasibility of Hexaminolevulinate based photodynamic therapy in patients with intermediate or high-risk transitional cell carcinoma of the bladder.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 1
About this study
Non-muscle invasive bladder cancer is currently treated by transurethral resection (TURB) and/or fulguration. However, recurrence and progression rates following endoscopic treatment of visible lesions are significant. To prevent recurrent and progressive disease, adjuvant intravesical chemotherapy and immunotherapy are applied. There is also increasing interest in new therapeutic strategies such as photodynamic therapy.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Male or female aged 18 years or above who have given written informed consent.
- Patients with intermediate or high-risk superficial bladder cancer, defined as low-grade early recurrence within 6 months after local chemotherapy or BCG, primary or recurrent high-grade disease (TaG3, TaG3 with CIS or CIS alone) or patients with primary T1G3 who are tumour free at second resection.
Exclusion criteria
- Patients with muscle invasive tumour
- Patients with bladder shrinkage
- Patients who have received prior PDT for bladder cancer
- History of T1G3 disease or other indications for cystectomy
- Patient with porphyria
- Gross haematuria. (Note: Gross haematuria is defined as a heavy bladder bleed resulting in marked amounts of blood in the urine, which may interfere with PDT)
- Patients who have received BCG or chemotherapy within three months prior to Hexvix instillation, except for a single dose of chemotherapy for prevention of seeding after resection
- Known allergy to hexaminolevulinate or a similar compound
- Participation in other clinical studies either concurrently or within the last 30 days
- Women of child-bearing potential.
- Conditions associated with a risk of poor protocol compliance
Treatment and study plan
Primary outcomes
-
Number of patients with adverse events
To assess the safety of photodynamic therapy (PDT) using Hexvix and the Karl Storz T-light PDT System in patients with recurrent bladder cancer.
(assessment of adverse events, blood biochemistry, vital signs, urodynamics)
Secondary outcomes
-
The number of tumour-free patients after 6 months
To assess the efficacy of Hexvix PDT in patients with intermediate and high-risk bladder cancer
Sponsors and collaborators
Lead sponsor
Photocure
Industry
Collaborators
- Karl Storz
Registry information
Official study title
A Phase I Feasibility Study of Hexvix Photodynamic Therapy in Patients With Intermediate or High-risk Bladder Cancer
Important dates
- Study start
- 2005
- Primary completion
- 2008
- Study completion
- 2008
- First posted
- Feb 25, 2011
- Registry last updated
- Feb 25, 2011
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.