An Observational Study of the Ethnic Impact of Patients Undergoing Second (2nd) Line Treatment for Non-Small Cell Lung Cancer Using Pemetrexed
NCT ID: NCT00497770
Last Updated: 2012-05-02
Study Results
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View full resultsBasic Information
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COMPLETED
434 participants
OBSERVATIONAL
2007-02-28
2011-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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PROSPECTIVE
Study Groups
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Caucasian
Caucasian patients receiving Alimta for 2nd line NSCLC
Pemetrexed
Treatment pattern and treatment initiation or changes are solely at the discretion of the physician and the patient
African American
African American patients receiving Alimta for 2nd line NSCLC
Pemetrexed
Treatment pattern and treatment initiation or changes are solely at the discretion of the physician and the patient
Asian American
Asian American patients receiving Alimta for 2nd line NSCLC
Pemetrexed
Treatment pattern and treatment initiation or changes are solely at the discretion of the physician and the patient
Hispanic
Hispanic patients receiving Alimta for 2nd line NSCLC
Pemetrexed
Treatment pattern and treatment initiation or changes are solely at the discretion of the physician and the patient
Interventions
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Pemetrexed
Treatment pattern and treatment initiation or changes are solely at the discretion of the physician and the patient
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Stage IIIB or IV disease
* Should have had 1 line of chemotherapy for Metastatic disease
* Adequate hematologic, hepatic and renal function
* Measurable or evaluable disease
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Eli Lilly and Company
INDUSTRY
Responsible Party
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Principal Investigators
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Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)
Role: STUDY_DIRECTOR
Eli Lilly and Company
Locations
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For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Mobile, Alabama, United States
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Glendale, Arizona, United States
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Anaheim, California, United States
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Campbell, California, United States
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Daly City, California, United States
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La Jolla, California, United States
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Lancaster, California, United States
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Mission Hills, California, United States
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Palo Alto, California, United States
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Poway, California, United States
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San Diego, California, United States
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San Francisco, California, United States
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San Jose, California, United States
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Santa Cruz, California, United States
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Sunnyvale, California, United States
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Denver, Colorado, United States
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Greeley, Colorado, United States
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Stamford, Connecticut, United States
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Fort Lauderdale, Florida, United States
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Miami, Florida, United States
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Weston, Florida, United States
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Decatur, Georgia, United States
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Honolulu, Hawaii, United States
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Kealakekua, Hawaii, United States
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Morehead, Kentucky, United States
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New Orleans, Louisiana, United States
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Omaha, Nebraska, United States
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Las Vegas, Nevada, United States
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Buffalo, New York, United States
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Washington, North Carolina, United States
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Memphis, Tennessee, United States
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Nashville, Tennessee, United States
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Corpus Christi, Texas, United States
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Galveston, Texas, United States
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Richardson, Texas, United States
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Monroe, Washington, United States
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Seattle, Washington, United States
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San Juan, , Puerto Rico
Countries
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Other Identifiers
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H3E-US-B001
Identifier Type: OTHER
Identifier Source: secondary_id
10733
Identifier Type: -
Identifier Source: org_study_id
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