Trial Information

Summary: Combination Chemotherapy Treatment For Advanced Non-Small Cell Lung Cancer Patients Having Prior Chemotherapy

The purpose of this study is to compare the efficacy and safety of a weekly regimen of two FDA approved drugs in combination versus one FDA approved drug in patients with advanced non-small cell lung cancer who have received one previous chemotherapy.

Inclusion Criteria (subjects must meet the following criteria in order to be considered eligible for this study):

  • Written informed consent
  • Confirmed advanced non-small cell lung carcinoma (NSCLC)
  • Received one prior chemotherapy for metastatic NSCLC. In addition, patients are allowed to have previously received a non-cytotoxic therapy, such as an endothelial growth factor receptor (EGFR) or angiogenesis inhibitor.
  • Presence of either measurable or non-measurable disease by radiologic study or physical examination.
  • Full recovery and at least 21 days from prior treatment for NSCLC.
  • At least 3 weeks since last major surgery (lesser period is acceptable if deemed in the best interest of the patient).
  • At least 7 days since prior radiotherapy.
  • Adequate bone marrow reserve, and adequate kidney and liver function.

Exclusion Criteria (subjects cannot meet the following criteria in order to be considered eligible for this study):

  • Symptoms of brain metastases requiring treatment with steroids.
  • Active infection.
  • Severe medical problems other than the diagnosis of NSCLC that would limit the ability of the patient to follow study guidelines or expose the patient to extreme risk.
  • Ongoing or planned chemotherapy (other than treatment during this study), immunotherapy, radiotherapy, or investigational therapy for the treatment of NSCLC.
  • Use of investigational drug within 30 days prior to the first dose of study medication.
  • Women who are pregnant or lactating.
  • Patients of child-bearing potential refusing to practice adequate contraception.
  • Patients who cannot receive steroid premedication.

Healthy Volunteers: no
Gender: Both
Minimum Age: 18 Years
Maximum Age: N/A

Contact:

Study Site
Located in:
Skokie, IL 60077
Telephone: 847-673-1999

 

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Trial listings updated: February 25, 2008 at 2:28:15 PM


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