12
Participants
Start Date
October 31, 2009
Primary Completion Date
November 30, 2012
Study Completion Date
November 30, 2012
cis-UCA solution
Cohort I: 2% cis-UCA solution (50 ml); min 3, max 12 patients
cis-UCA solution
Cohort II: 4% cis-UCA solution (50 ml); min 0, max 12 patients
cis-UCA solution
Cohort III: 6% cis-UCA solution (50 ml); min 0, max 12 patients
Turku University Hospital, Department of Surgery, Division of Urology, Turku
Tampere University Hospital, Department of Urology, Tampere
Lead Sponsor
Turku University Hospital
OTHER_GOV
Tampere University Hospital
OTHER
FinnMedi Oy
INDUSTRY
BioCis Pharma Ltd
INDUSTRY