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Comparing 3 Schedules of Alimta Plus Gemzar

Phase 2
Completed
Conditions
Carcinoma, Non-Small-Cell Lung
Lung Neoplasms
Neoplasms
Registration Number
NCT00034606
Lead Sponsor
Eli Lilly and Company
Brief Summary

The purpose of the study is to measure tumor response rates for three schedules of Alimta(LY231514) in combination with gemcitabine in patients with locally advanced or metastatic non small cell lung cancer who have received no prior chemotherapy regimen.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Diagnosis of non-small lung cancer
  • No prior chemotherapy
  • Able to care for self
Exclusion Criteria
  • An ongoing infection
  • Pregnancy or breast feeding
  • Other serious medical condition
  • Cancer that has spread to the brain
  • Inability to take folic acid

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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