A randomised clinical trial investigating the effect of durvalumab versus nil in patients with locally-advanced or metastatic urothelial carcinoma of the bladder who had progressed while on or after a platinum-containing chemotherapy, including those who progressed within 12 months of receiving therapy in a neoadjuvant or adjuvant setting
Studied treatment | durvalumab at 10 mg/kg body weight administered as an intravenous infusion over 60 minutes every two weeks until disease progression or unacceptable toxicity |
Control treatment |
Patients | patients with locally-advanced or metastatic urothelial carcinoma of the bladder who had progressed while on or after a platinum-containing chemotherapy, including those who progressed within 12 months of receiving therapy in a neoadjuvant or adjuvant setting |
Group sizes | -9 / -9 |
Blindness | Inclusion period | ||
Follow-up duration | Centers | ||
Lost to FU | geographical localisation | ||
Primary endpoint | Design | Single-arm study |
phase 1/2
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Appears in following systematic reviews: