A Randomized, Comparative Study of Hexvix Fluorescence Cystoscopy and Standard Cystoscopy in Patients With Non-invasive Bladder Cancer
Launched by PHOTOCURE · Dec 18, 2006
Trial Information
Current as of May 25, 2025
Completed
Keywords
ClinConnect Summary
The main objective of the study is to compare the 1-year recurrence rate of Hexvix assisted Transuretheral Resection of the Bladder (TURB) to standard white light TURB in patients with suspicion of non-invasive bladder cancer.
Patients will be followed 4, 8 and 12 months after the initial TURB. This follow-up regimen is according to standard clinical practice in Denmark.
Recurrence of non-invasive bladder cancer is frequent, and this study is designed to investigate whether Hexvix assisted TURB can reduce the early recurrence compared to standard TURB
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patients with suspicion of non-invasive bladder cancer indicated for a transuretheral resection of the bladder
- • Above 18 years
- • Written informed consent obtained
- Exclusion Criteria:
- • Gross hematuria. (Note: Gross hematuria is defined as a heavy bladder bleed resulting in marked amounts of blood in the urine, which may interfere with fluorescence cystoscopy. Where the bleed is light, the patient should not be excluded if in the investigator's opinion, rinsing during cystoscopy will alleviate the possible interference with fluorescence cystoscopy).
- • Patient with porphyria.
- • Known allergy to hexyl aminolevulinate hydrochloride or a similar compound.
- • Participation in other clinical studies with investigational drugs either concurrently or within the last 30 days.
- • Pregnant or breast-feeding (all women of child-bearing potential must document a negative serum or urine pregnancy test at screening and use the contraceptive pill or intrauterine device (IUD) during the treatments and for at least one month thereafter).
- • Conditions associated with a risk of poor protocol compliance.
About Photocure
Photocure is a pioneering biopharmaceutical company focused on developing innovative photodynamic therapy (PDT) solutions for the diagnosis and treatment of cancer. With a commitment to enhancing patient outcomes through advanced therapeutic modalities, Photocure leverages its proprietary technology to create targeted treatments that minimize side effects and improve quality of life. The company is dedicated to rigorous clinical research and collaboration with healthcare professionals, ensuring that its therapies are backed by robust scientific evidence and meet the highest standards of safety and efficacy. Through its groundbreaking work, Photocure aims to transform the landscape of cancer care and provide new hope for patients worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Odense, , Denmark
Odense, , Denmark
Frederiksberg, , Denmark
Patients applied
Trial Officials
Gregers G Hermann, MD, DM Sci
Principal Investigator
Frederiksberg Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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