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A Phase III, Multi-center, Randomized Trial of Pemetrexed and Gefitinib in Never-smoker and Adenocarcinoma Patients With Non-small Cell Lung Cancer Previously Treated With Platinum-based Chemotherapy


Phase 3
18 Years
N/A
Open (Enrolling by invite only)
Both
Non-small Cell Lung Cancer

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Trial Information

A Phase III, Multi-center, Randomized Trial of Pemetrexed and Gefitinib in Never-smoker and Adenocarcinoma Patients With Non-small Cell Lung Cancer Previously Treated With Platinum-based Chemotherapy


Inclusion Criteria:



1. Histologically confirmed pulmonary adenocarcinoma including bronchioloalveolar, but
except adenosquamous cell carcinoma

2. Stage IIIB (malignant pleural effusion and/or pleural seeding), stage IV and relapsed
non-small cell lung cancer

3. Failed with 1st line platinum-based chemotherapy or relapsed within 12 months after
adjuvant platinum-based chemotherapy)

4. Never smoker (less than 100 cigarette for the life time)

5. 18 year or older

6. ECOG 0-2

7. No history of biologic or immunotherapy

8. Tolerable renal function ( creatine clearance rate is 60ml/min or more)

9. Tolerable hepatic function (Serum bilirubin ≤ 1.25 x UNL, AST (SGOT) and ALT (SGPT) ≤
2.5 x UNL, alkaline phosphatase ≤5 x UNL)

Exclusion Criteria:

1. symptomatic brain metastasis

2. previously treated with EGFR tyrosine kinase inhibitor

3. previously treated with antifolate agents

4. poor oral absorption

5. patients with active infection

6. uncontrolled diabetes mellitus

7. significant cardiovascular disease (uncontrolled hypertension, history of myocardial
infarction or unstable angina within 6 months, congestive heart failure)

8. pregnant or nursing patients

9. history of malignant disease within 3 years before the enrollment except for cured
non-melanomatous skin cancer, cervical carcinoma in situ, or thyroid carcinoma

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

progression-free survival

Outcome Time Frame:

36 months

Safety Issue:

No

Principal Investigator

Myungju Ahn, Ph.D., M.D.

Investigator Role:

Principal Investigator

Investigator Affiliation:

Samsung Medical Center

Authority:

Korea: Food and Drug Administration

Study ID:

2008-04-030

NCT ID:

NCT01066195

Start Date:

May 2008

Completion Date:

Related Keywords:

  • Non-Small Cell Lung Cancer
  • Non-Small Cell Lung Cancer
  • Never-Smoker and Adenocarcinoma patients
  • Pemetrexed (ALIMTA)
  • Gefitinib (IRESSA®)
  • Adenocarcinoma
  • Adenocarcinoma, Mucinous
  • Carcinoma, Non-Small-Cell Lung
  • Lung Neoplasms

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