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Clinical Trial Summary

This study aims to assess objective response rate of modified FOLFIRINOX in advanced urachaus cancer. Patients with locally advanced, recurrent, or metastatic urachal carcinoma of bladder, urachal will be enrolled this study. Modified version of FOLFIRINOX(Oxaliplatin 85 mg/m 2, Leucovorin 400mg/m2 , irinotecan 150mg/m2 and 5-FU 2400mg/m2) with prophylactic pegateograstim will be continued till progression, unacceptable toxicity, or till 12 cycles (24 weeks). Study drugs can be administered after 12 cycles to the subjects with benefit from study medication. Response evaluation will be done every 6 weeks.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04611724
Study type Interventional
Source Asan Medical Center
Contact Jae -Lyun Lee, Professor
Phone 82 2 3010 5977
Email jaelyun@amc.seoul.kr
Status Recruiting
Phase Phase 2
Start date December 1, 2020
Completion date September 30, 2024

See also
  Status Clinical Trial Phase
Active, not recruiting NCT00082706 - Fluorouracil, Leucovorin, Gemcitabine, and Cisplatin in Treating Patients With Metastatic or Unresectable Adenocarcinoma of the Urothelium or Urachal Remnant Phase 2