Status:

COMPLETED

Study Comparing Short Infusion Vs. Fixed Dose of Cisplatin + Gemcitabine in Non Small Cell Lung Cancer.

Lead Sponsor:

Eli Lilly and Company

Conditions:

Non-Small-Cell Lung Carcinoma

Eligibility:

All Genders

18+ years

Phase:

PHASE2

Brief Summary

The purposes of this study are to determine: How standard gemcitabine plus cisplatin compares to fixed dose rate of gemcitabine plus cisplatin in the treatment of non-small cell lung cancer. The saf...

Eligibility Criteria

Inclusion

  • At least 18 years of age
  • Histologically or cytologically confirmed diagnosis of NSCLC
  • Have provided written informed consent
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1
  • Adequate organ function

Exclusion

  • Prior chemotherapy or biologic therapy (approved or experimental) for NSCLC
  • Presence of uncontrolled central nervous system (CNS) metastases
  • Inability to comply with protocol or study procedures
  • Pregnancy
  • Breast feeding

Key Trial Info

Start Date :

March 1 2004

Trial Type :

INTERVENTIONAL

End Date :

May 1 2006

Estimated Enrollment :

64 Patients enrolled

Trial Details

Trial ID

NCT00191620

Start Date

March 1 2004

End Date

May 1 2006

Last Update

January 26 2007

Active Locations (4)

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Page 1 of 1 (4 locations)

1

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

Buenos Aires, Argentina

2

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

São Paulo, Brazil

3

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

Santiago, Chile

4

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

Mexico City, Mexico