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Tarceva With or Without Apatinib in the Advanced Lung Adenocarcinoma

Primary Purpose

Lung Cancer

Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Apatinib
Tarceva
Placebo
Sponsored by
First Affiliated Hospital of Kunming Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lung Cancer

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • lung adenocarcinoma proved by histology;with mutant EGFR;ECOG PS 0-2;Clinical stage IIIb or IV;without other fatal disease;without hemorrhagic disease;normal liver,renal and bone marrow function,not pregnant.

Exclusion Criteria:

  • ECOG PS 3-5;abnormal liver,renal and bone marrow function,pregnant;with severe diseases;wild type EGFR

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Placebo Comparator

    Experimental

    Arm Label

    TarceP

    TarceA

    Arm Description

    Tarceva with Placebo

    Tarceva with Apatinib

    Outcomes

    Primary Outcome Measures

    Progression free survival
    From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 36 months

    Secondary Outcome Measures

    Overall survival
    From date of randomization until the date of death from any cause, assessed up to 36 months
    Response rate

    Full Information

    First Posted
    February 27, 2016
    Last Updated
    March 9, 2016
    Sponsor
    First Affiliated Hospital of Kunming Medical University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02704767
    Brief Title
    Tarceva With or Without Apatinib in the Advanced Lung Adenocarcinoma
    Official Title
    Tarceva With or Without Apatinib in the First-line Therapy of Advanced Lung Adenocarcinoma With Mutant EGFR:a Phase II Study.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2016
    Overall Recruitment Status
    Unknown status
    Study Start Date
    June 2016 (undefined)
    Primary Completion Date
    June 2019 (Anticipated)
    Study Completion Date
    December 2019 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    First Affiliated Hospital of Kunming Medical University

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Tarceva now was established first-line therapy for advanced lung adenocarcinoma with mutant EGFR patients.However,the benefit lasted for about 6-8 months.So we consider to add apatinib,a tyrosine kinase inhibitor of VEGF,to the therapy of these patients.
    Detailed Description
    Lung adenocarcinoma is the most common NSCLC,most patient were diagnosed to advanced stage.The first-line therapy include chemotherapy of targeted therapy .Tarceva now was established first-line therapy for advanced lung adenocarcinoma with mutant EGFR patients.However,the benefit lasted for about 6-8 months.So we consider to add apatinib,a tyrosine kinase inhibitor of VEGF,to the therapy of these patients.We designed the study to find out whether the addition of apatinib to the Tarceva would enhance the efficacy of Tarceva.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Lung Cancer

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Allocation
    Randomized
    Enrollment
    60 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    TarceP
    Arm Type
    Placebo Comparator
    Arm Description
    Tarceva with Placebo
    Arm Title
    TarceA
    Arm Type
    Experimental
    Arm Description
    Tarceva with Apatinib
    Intervention Type
    Drug
    Intervention Name(s)
    Apatinib
    Other Intervention Name(s)
    AiTan
    Intervention Description
    a tyrosine kinase inhibitor of VEGF invented by Hengrui pharma in China
    Intervention Type
    Drug
    Intervention Name(s)
    Tarceva
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Primary Outcome Measure Information:
    Title
    Progression free survival
    Description
    From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 36 months
    Time Frame
    From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 36 months
    Secondary Outcome Measure Information:
    Title
    Overall survival
    Description
    From date of randomization until the date of death from any cause, assessed up to 36 months
    Time Frame
    From date of randomization until the date of death from any cause, assessed up to 36 months
    Title
    Response rate
    Time Frame
    through study completion, an average of 1 year

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: lung adenocarcinoma proved by histology;with mutant EGFR;ECOG PS 0-2;Clinical stage IIIb or IV;without other fatal disease;without hemorrhagic disease;normal liver,renal and bone marrow function,not pregnant. Exclusion Criteria: ECOG PS 3-5;abnormal liver,renal and bone marrow function,pregnant;with severe diseases;wild type EGFR

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided
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    Tarceva With or Without Apatinib in the Advanced Lung Adenocarcinoma

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