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
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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