ALIMTA (Pemetrexed) Alone or in Combination With Cisplatin for Patients With Malignant Mesothelioma.

Sponsor
Eli Lilly and Company (Industry)
Overall Status
Approved for marketing
CT.gov ID
NCT00040625
Collaborator
(none)
6

Study Details

Study Description

Brief Summary

This study is to evaluate the effects (good and bad) of ALIMTA and Cisplatin or ALIMTA alone on you and your malignant pleural mesothelioma as well as make ALIMTA available to patients who qualify for treatment.

Condition or Disease Intervention/Treatment Phase

Study Design

Study Type:
Expanded Access

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Have a proven diagnosis of malignant mesothelioma in patients not candidates for curative surgery

    • Prior chemotherapy for your disease is allowed

    • Measurable lesion is not required

    • Have a adequate performance status

    • Sign an informed consent form

    Exclusion Criteria:
    • You are excluded from this trial if you have received any investigational agent within 4 week before enrolling in this study

    • You are excluded from this trial if you have received radiation within the previous 2 weeks

    • You are excluded from this trial if you are a candidates for curative surgery

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY(1-877-285-4559) or speak with your personal physician. Basking Ridge New Jersey United States
    2 For additional information regarding investigative sites for this trial, contact the Clinical Trials support Center at 1-877-CTLILLY (1-877-285-4559) or speak with your personal physician Porto Alegre RS Brazil
    3 For additional information regarding investigative sites for this trial, contact the Clinical Trials support Center at 1-877-CTLILLY (1-877-285-4559) or speak with your personal physician Sao Paulo Brazil
    4 "For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-285-4559) or speak with your personal physician." Cairo Egypt
    5 For additional information regarding investigative sites for this trial, contact the Clinical Trials support Center at 1-877-CTLILLY (1-877-285-4559) or speak with your personal physician Cairo Egypt
    6 For additional information regarding investigative sites for this trial, contact the Clinical Trials support Center at 1-877-CTLILLY (1-877-285-4559) or speak with your personal physician Jeddah Saudi Arabia

    Sponsors and Collaborators

    • Eli Lilly and Company

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00040625
    Other Study ID Numbers:
    • 6093
    • H3E-US-JMFE
    First Posted:
    Jul 4, 2002
    Last Update Posted:
    Mar 15, 2007
    Last Verified:
    Mar 1, 2007
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 15, 2007