Enzastaurin as Second and Third-Line Treatment for Non-Small Cell Lung Cancer.
NCT ID: NCT00105092
Last Updated: 2007-05-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
50 participants
INTERVENTIONAL
2005-03-31
2007-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Interventions
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Enzastaurin HCL
Eligibility Criteria
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Inclusion Criteria
* Must have been diagnosed with advanced or metastatic non-small cell lung cancer
* Must be able to visit the doctor's office every 28 days for 6 months or longer.
Exclusion Criteria
* Have other significant medical problems as determined by your physician
* Are unable to swallow tablets
* Have a history of significant heart disease
18 Years
ALL
No
Sponsors
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Eli Lilly and Company
INDUSTRY
Principal Investigators
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Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM to 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.
Tampa, Florida, United States
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.
Nashville, Tennessee, United States
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.
Houston, Texas, United States
Countries
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Other Identifiers
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H6Q-MC-JCAQ
Identifier Type: -
Identifier Source: secondary_id
8670
Identifier Type: -
Identifier Source: org_study_id