Molecularly Target Therapy With FORFIRINOX in Advanced or Recurrent Extrahepatic Cholangiocarcinoma and Gallbladder Carcinoma

NCT03768375 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2018-12-07

No results posted yet for this study

Summary

The purpose of this study is to evaluate the feasibility, efficacy and safety of target therapy according to genomic and proteomic profiling combined with FORFIRINOX in advanced or recurrent extrahepatic cholangiocarcinoma and gallbladder carcinoma.

Conditions

  • Cholangiocarcinoma of the Extrahepatic Bile Duct
  • Gallbladder Cancer

Interventions

BIOLOGICAL

conventional chemotherapy(FORFIRINOX) combined with target agents

Drug: FORFIRINOX Conventional chemotherapy:gemcitabine and oxaliplatin Drug: Cetuximab Drug: Trastuzumab Drug: Gefitinib Drug: Lapatinib Drug: Everolimus Drug: Sorafenib Drug: Crizotinib

BIOLOGICAL

conventional chemotherapy(FORFIRINOX)

conventional chemotherapy(FORFIRINOX)

Sponsors & Collaborators

  • Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

    collaborator OTHER
  • Ruijin Hospital

    collaborator OTHER
  • RenJi Hospital

    collaborator OTHER
  • Eastern Hepatobiliary Surgery Hospital

    collaborator OTHER
  • Huashan Hospital

    collaborator OTHER
  • Shanghai Jiao Tong University School of Medicine

    lead OTHER

Principal Investigators

  • yingbin liu, PHD · Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-11-30
Primary Completion
2020-12-30
Completion
2021-12-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03768375 on ClinicalTrials.gov