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

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

434 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-02-28

Study Completion Date

2011-03-31

Brief Summary

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This large, non-randomized observational study is being conducted to provide data about the impact of ethnic origin on outcomes and resource utilization during the 2nd line treatment of non-small cell lung cancer (NSCLC) in a routine medical care setting.

Detailed Description

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This is a large 1000 patient single arm observational study being conducted to determine the impact of ethnic origin (Caucasian, African-Americans, Asian-Americans, and Hispanics) on patients being treated for 2nd line advanced NSCLC with pemetrexed given in routine clinical practice. Data will be collected on disease control rate by pemetrexed as defined by Response Rate (RR) (Complete Response (CR) + Partial Response (PR)), Stable Disease (SD) and toxicities. In addition, overall survival, progression-free survival, treatment toxicities, activities of daily living, symptom burden and resource utilization will also be observed. To meet the study goals, a total of 400 Caucasians, 200 African- Americans, 200 Asian-Americans, and 200 Hispanics will be accrued to this study.

Conditions

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Lung Neoplasms

Study Design

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Study Time Perspective

PROSPECTIVE

Study Groups

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Caucasian

Caucasian patients receiving Alimta for 2nd line NSCLC

Pemetrexed

Intervention Type DRUG

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

Intervention Type DRUG

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

Intervention Type DRUG

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

Intervention Type DRUG

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

Intervention Type DRUG

Other Intervention Names

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LY231514 Alimta

Eligibility Criteria

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Inclusion Criteria

* Non-small cell lung cancer (NSCLC) (any histologic type)
* 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

* Pregnant or lactating females
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Eli Lilly and Company

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

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Glendale, Arizona, United States

Site Status

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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

Site Status

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Galveston, Texas, United States

Site Status

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Richardson, Texas, United States

Site Status

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Monroe, Washington, United States

Site Status

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Seattle, Washington, United States

Site Status

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San Juan, , Puerto Rico

Site Status

Countries

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United States Puerto Rico

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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