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Clinical Trials/JPRN-UMIN000004680
JPRN-UMIN000004680
Recruiting
Phase 2

A Phase II Study of Erlotinib for previously treated Non-Small Cell Lung Cancer Patients - A Phase II Study of Erlotinib for previously treated Non-Small Cell Lung Cancer Patients

Tottori University, Faculty of Medicine,Division of Medical Oncology and Molecular Respirology Department of Multidisciplinary Internal Medicine0 sites27 target enrollmentDecember 8, 2010

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Objective of the study is to investigate efficacy and safety of Erlotinib for previously treated non-small cell lung cancer patients.
Sponsor
Tottori University, Faculty of Medicine,Division of Medical Oncology and Molecular Respirology Department of Multidisciplinary Internal Medicine
Enrollment
27
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 8, 2010
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Tottori University, Faculty of Medicine,Division of Medical Oncology and Molecular Respirology Department of Multidisciplinary Internal Medicine

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) Patients with active lung disease such as interstitial pneumonia, pneumoconiosis, active radiation pneumonitis, or drug\-induced pneumonitis. 2\) Patients with massive pleural or pericardial effusion,or ascites. 3\) Patients with active severe infections. 4\) Cases with past history of administration of HER related agents(gefitinib,trastuzumab,lapatinib,cetuximab). 5\) Impossible cases with oral administration. 6\) Patients with active opthalmological disease. 7\) Pregnancy or lactation. 8\) Patients with symptomatic brain metastasis. 9\) Patients with active concomitant malignancy. 10\) Patients with uncontrollabe diabetes mellitus. 11\) Patients with uncontrollable complications. 12\) Inappropriate patients for this study judged by the physicians.

Outcomes

Primary Outcomes

Not specified

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