drugset / Trial / NCT07184021

Neoadjuvent Dose-dense Gemcitabine and Cisplatin In Muscle Invasive Bladder Cancer

NCT07184021 ↗

Phase 2 Not yet recruiting 30 enrolled Assiut University
NaSingle-groupOpen-labelTreatment

Summary

To evaluate the feasibility, safety, and pathological response of dose-dense neoadjuvant gemcitabine and cisplatin in patients with muscle-invasive bladder cancer, with the goal of improving tumor downstaging and optimizing outcomes before radical cystectomy.

Timeline

Start
2025-09
Primary completion
2027-09
Completion
2027-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Cisplatin Other / unclassified 35 mg/m2 Intravenous
Subject Gemcitabine Small molecule 1200 mg/m2 Intravenous