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Chemotherapy mFOLFIRINOX in Locally Advanced or Metastatic Cholangiocarcinoma

S

Shanghai Jiao Tong University School of Medicine

Status

Unknown

Conditions

Cholangiocarcinoma of the Bile Duct

Study type

Observational

Funder types

Other

Identifiers

NCT04305288
CCA20191021

Details and patient eligibility

About

The aim of this study was to evaluate the effectiveness of modified FOLFIRINOX (mFOLFIRINOX) compared to that of gemcitabine plus oxaliplatin (Gemox) for patients with locally advanced or metastatic CCA

Full description

The aim of this study was to evaluate the effectiveness of modified FOLFIRINOX (mFOLFIRINOX) compared to that of gemcitabine plus oxaliplatin (Gemox) for patients with locally advanced or metastatic CCA

Enrollment

100 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

The inclusion criteria included: patients aged 18-70 years old, regardless of gender; patients with locally advanced or metastatic CCA diagnosed by imaging and pathology; modified FOLFIRINOX regimen or Gemox regimen as first-line treatment; ≥ 1 focus that can be evaluated by imaging examination.

Exclusion criteria included: incomplete clinical history data; suffering from other malignant tumors within 5 years, except basal cell carcinoma and cervical carcinoma in situ; having received other systemic chemotherapy, targeted therapy, immunotherapy or radiotherapy as first-line treatment; with severe organ dysfunction.

Trial design

100 participants in 2 patient groups

Gemox
Description:
The patients received conventional chemotherapy Gemox
mFOLFIRINOX
Description:
The patients received chemotherapy modified FOLFIRINOX

Trial contacts and locations

1

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Central trial contact

yingbin liu, PHD

Data sourced from clinicaltrials.gov

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