About this trial

The goal of this single arm, prospective, open-label, investigator-initiated Phase 2 clinical trial is to evaluate the efficacy of intravesical chemoablation in patients with low grade bladder cancer.

Eligibility criteria

Qualifiers

Male/female participants who are at least 18 years of age on the day of providing documented informed consent will be enrolled in this study

Diagnosis of a recurrent tumor and a history of TaLG BCa or diagnosis of primary TaLG BCa histologically confirmed by cold cup biopsy at screening or within 8 weeks before screening

On screening cystoscopy: Diameter of the largest lesion ≤15mm

Number of lesions ≤5

Disqualifiers

Tumors that clinicians suspect to be HG

Positive HG cytology according to Paris criteria

Diameter of tumor >15 mm

Number of lesions >5

Trial design

Treatments tested in this trial

  • Gemcitabine

Treatment groups

47 Participants
are divided into 1 treatment group

Locations

1
Department of Urology, Medical University of Vienna1090, Vienna Austria

Sponsors and collaborators

Ekaterina Laukhtina

Lead sponsor

Medical University of Vienna

Sponsor institution