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G-DISCO

 Bladder — In Follow-up

The purpose of the study is to determine the safety feasibility and tolerability of synchronous gemcitabine docetaxel administration into the bladder.

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TRIAL TITLE

A Phase 1 study of feasibility, safety and tolerability of synchronous intravesical administration of gemcitabine and docetaxel

CONSUMER TITLE

Early-phase study testing whether giving two chemotherapy treatments (gemcitabine and docetaxel) directly into the bladder together is safe and well tolerated for people with bladder cancer.

CANCER TYPE

Bladder

TRIAL STATUS

In Follow-up

PROTOCOL NUMBER

ANZUP 2403

CO-ORDINATING CENTRE

STUDY CHAIR

Dickon Hayne, Cynthia Hawks

PATIENT POPULATION

Males and females aged 18 years and over who have fully resected high-risk non-muscle-invasive bladder cancer (HRNMIBC) that is unresponsive to intravesical therapy, an ECOG status of 0-2, a life expectancy of > 6 months, and adequate organ and bone marrow function.

RECRUITMENT TARGET

15 people

ACKNOWLEDGEMENT

The study is funded by a Below the Belt grant awarded by the Australian and New Zealand Urogenital and Prostate (ANZUP) Cancer Trials Group.

DETAILED INFORMATION

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