Effectiveness of Hexaminolevulinate (Hexvix) in the Diagnosis and Treatment of Patients With Non-invasive Bladder Cancer

CompletedOBSERVATIONAL
Enrollment

283

Participants

Timeline

Start Date

February 29, 2008

Primary Completion Date

September 30, 2010

Study Completion Date

September 30, 2010

Conditions
Bladder Cancer
Interventions
DRUG

Hexaminolevulinate (Hexvix)

Each patient enrolled into the study will be infused with 50 mL of a 2 mg/mL Hexvix solution in the bladder using a catheter. Subsequently, after fluid retention by the patient in the bladder for one hour, the bladder will be emptied.

Trial Locations (1)

28108

GE Healthcare, Madrid

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GE Healthcare

INDUSTRY