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EXIBIT: Oxaliplatin in Biliary Tract Cancer

Primary Purpose

Biliary Tract Neoplasms

Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
oxaliplatin
Sponsored by
Sanofi
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Biliary Tract Neoplasms

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Histologically proven, locally advanced or metastatic carcinoma of the biliary tract (gallbladder, intrahepatic bile ducts, extrahepatic bile ducts, ampula of Vater) For intrahepatic bile ducts, if the diagnosis of biliary tract origin is not evident by imaging or surgical exploration, and so equivalent to liver metastasis with unknown primary site, inclusion is possible if: unknown primary after an exhaustive search for the primary site (chest radiography- , thoracic and abdomino pelvic CT scan, colonoscopy, oesogastroduodenal endoscopy, PSA determination for men or mammography for women, and PET scan if possible). histological examination compatible with adenocarcinoma of bile ducts with the immunostaining expression of cytokeratin : 7+, 20- and 19 +. (Shimonishi, 2000 ^22) No prior chemotherapy for advanced disease (first line) No radiation therapy within 4 weeks prior to the first gemcitabine administration. Unidimensionally measurable disease. For female patient of childbearing potential, neither pregnant nor breastfeeding, and under active contraception No known allergy to one of the study drugs No prior malignancy No CNS metastases No peripheral neuropathy > grade 2 ECOG PS <=2 ANC > 1.5 X 10^9 /L Platelets > 100 X 10^9 /L Creatinine < 1.5 x ULN SGPT (ALT) < 5 x ULN Bilirubin < 2.5 x ULN (patients with jaundice or evidence of bile duct obstruction and in whom the biliary tree can be decompressed by endoscopic percutaneous endoprothesis, with subsequent reduction in bilirubin < 2.5 x ULN will be eligible for the study).

Sites / Locations

    Outcomes

    Primary Outcome Measures

    To evaluate response rate according to RECIST criteria

    Secondary Outcome Measures

    To evaluate the progression-free survival in the ITT population
    To investigate safety using NCI-CTC criteria version 2

    Full Information

    First Posted
    September 9, 2005
    Last Updated
    February 15, 2012
    Sponsor
    Sanofi
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00174564
    Brief Title
    EXIBIT: Oxaliplatin in Biliary Tract Cancer
    Official Title
    A Multicentre Phase II Trial of Gemcitabine and Oxaliplatin (GEMOX) in Patients With Biliary Tract Cancer
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2012
    Overall Recruitment Status
    Completed
    Study Start Date
    April 2003 (undefined)
    Primary Completion Date
    September 2006 (Actual)
    Study Completion Date
    September 2006 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Sanofi

    4. Oversight

    5. Study Description

    Brief Summary
    The primary objective is to evaluate the efficacy of the GEMOX treatment as 1st line therapy in patients with advanced biliary tract cancer based on response rate measured by the RECIST unidimensional criteria. Secondary objectives are : Progression free survival, overall survival and safety.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Biliary Tract Neoplasms

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    Non-Randomized
    Enrollment
    67 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    oxaliplatin
    Primary Outcome Measure Information:
    Title
    To evaluate response rate according to RECIST criteria
    Secondary Outcome Measure Information:
    Title
    To evaluate the progression-free survival in the ITT population
    Title
    To investigate safety using NCI-CTC criteria version 2

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Histologically proven, locally advanced or metastatic carcinoma of the biliary tract (gallbladder, intrahepatic bile ducts, extrahepatic bile ducts, ampula of Vater) For intrahepatic bile ducts, if the diagnosis of biliary tract origin is not evident by imaging or surgical exploration, and so equivalent to liver metastasis with unknown primary site, inclusion is possible if: unknown primary after an exhaustive search for the primary site (chest radiography- , thoracic and abdomino pelvic CT scan, colonoscopy, oesogastroduodenal endoscopy, PSA determination for men or mammography for women, and PET scan if possible). histological examination compatible with adenocarcinoma of bile ducts with the immunostaining expression of cytokeratin : 7+, 20- and 19 +. (Shimonishi, 2000 ^22) No prior chemotherapy for advanced disease (first line) No radiation therapy within 4 weeks prior to the first gemcitabine administration. Unidimensionally measurable disease. For female patient of childbearing potential, neither pregnant nor breastfeeding, and under active contraception No known allergy to one of the study drugs No prior malignancy No CNS metastases No peripheral neuropathy > grade 2 ECOG PS <=2 ANC > 1.5 X 10^9 /L Platelets > 100 X 10^9 /L Creatinine < 1.5 x ULN SGPT (ALT) < 5 x ULN Bilirubin < 2.5 x ULN (patients with jaundice or evidence of bile duct obstruction and in whom the biliary tree can be decompressed by endoscopic percutaneous endoprothesis, with subsequent reduction in bilirubin < 2.5 x ULN will be eligible for the study).
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Jean-Philippe Aussel
    Organizational Affiliation
    Sanofi
    Official's Role
    Study Director

    12. IPD Sharing Statement

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    EXIBIT: Oxaliplatin in Biliary Tract Cancer

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