PHASE 3, RANDOMIZED, OPEN-LABEL STUDY OF THE EFFICACY AND SAFETY OF PF-02341066 VERSUS STANDARD OF CARE CHEMOTHERAPY (PEMETREXED OR DOCETAXEL) IN PATIENTS WITH ADVANCED NONSMALL CELL LUNG CANCER (NSCLC) HARBORING A TRANSLOCATION OR INVERSION EVENT INVOLVING THE ANAPLASTIC LYMPHOMA KINASE (ALK) GENE LOCUS - ND

• Conditions: treatment of locally advanced or metastatic non-small cell lung cancer after failure of one prior chemotherapy regimen in patients with tumors harboring a translocation or inversion event involving the ALK gene locus.; MedDRA version: 12.1Level: LLTClassification code 10061873Term: Non-small cell lung cancer

• Registration Number: EUCTR2009-012595-27-IT
• Lead Sponsor: Pfizer Inc. 235 East 42nd Street, New York, NY 10017

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2009-12-23
• Last Update Posted: 11 April 2016

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: All
• Target Recruitment: 318

Inclusion Criteria

1. Histologically or cytologically proven diagnosis of NSCLC that is locally advanced or metastatic 2. Positive for translocation or inversion events involving the ALK gene locus (e.g. resulting in EML4-ALK fusion) as determined by an ALK break apart FISH assay and defined by an increase in the distance of 5 and 3 ALK probes or the loss of the 5 probe 3. Patients must have had progressive disease after only one prior chemotherapy regimen. This regimen must have been platinum-based and may have included maintenance therapy. Patients must be considered appropriate candidates for additional chemotherapy with either single-agent pemetrexed or single-agent docetaxel. - Includes patients who received one prior platinum-based chemotherapy for treatment of de novo Stage IIIB/IV NSCLC. - Includes patients who have received one prior platinum-based chemotherapy in the adjuvant setting following surgical resection for early disease and whose disease has recurred within 6 months of completion of prior chemotherapy - Includes patients who received one prior platinum-based chemotherapy in combination with radiation therapy for Stage III locoregional disease and whose disease has recurred within 6 months of completion of prior chemotherapy - Includes patients who received 2 prior platinum-based chemotherapy regimens, if the first regimen was given as adjuvant therapy or was given in combination with radiation therapy for locally advanced disease - Includes patients who have received prior treatment with an EGFR tyrosine kinase inhibitor, such as erlotinib or gefitinib, providing these patients have also received only one prior platinum-based chemotherapy regimen as in one of the scenarios described above 4. Patients with brain metastases are eligible if appropriately treated and neurologically stable for at least 2 weeks and is not taking any medications contraindicated in Exclusion Criteria #11-12 5. Any prior chemotherapy or major surgeries must have been completed at least 4 weeks prior to initiation of study medication. Any prior radiation or minor surgeries/procedures must have been completed at least 2 weeks prior to the initiation of study medication. Any acute toxicity must have recovered to ≤ Grade 1 (except alopecia) 6. Tumors must be measurable as per RECIST (version 1.0) - At least one target lesion and which is measurable in at least one dimension of ≥ 20 mm by conventional computerized tomography (CT) or magnetic resonance imaging (MRI), or ≥ 2 x the reconstruction interval by spiral CT must be present - Target lesions can be chosen from a previous irradiated area if lesions in those areas have documented progression 7. Female or male, 18 years of age or older 8. ECOG performance status 0-2 9. Adequate organ function as defined by the following criteria: Hepatic function - Serum aspartate transaminase (AST) and serum alanine transaminase (ALT) 1.5 x ULN concomitant with alkaline phosphatase > 2.5 x ULN - Total serum bilirubin </=1.5 x ULN (except patients with documented Gilbert s syndrome); however for patients who if randomly assigned to Arm B must receive docetaxel, total serum bilirubin must be ≤ 1 x ULN Bone marrow function

Exclusion Criteria

1. Current treatment on another therapeutic clinical trial 2. Prior therapy specifically directed against ALK 3. Spinal cord compression, carcinomatous meningitis, or leptomeningeal disease 4. Any of the following within the 6 months prior to starting study treatment: myocardial infarction, severe/unstable angina, coronary/peripheral artery bypass graft, congestive heart failure, or cerebrovascular accident including transient ischemic attack. 5. Ongoing cardiac dysrhythmias of NCI CTCAE Grade >/=2, atrial fibrillation of any grade, or QTc interval >470 msec 6. Previous treatment with PF-02341066 7. Patients who if randomly assigned to Arm B must receive pemetrexed and who have NSCLC with predominantly squamous cell carcinoma 8. Patients who if randomly assigned to Arm B must receive docetaxel and who have peripheral neuropathy with Grade > 2 (CTCAE version 3.0) 9. Patients who if randomly assigned to Arm B must receive docetaxel and who are receiving concomitant medications formulated with polysorbate 80 10. Hypertension that cannot be controlled by medications (>150/100 mmHg despite optimal medical therapy) 11. Pregnancy or breastfeeding. 12. Use of drugs or foods that are known potent CYP3A4 inhibitors, including but not limited to amprenavir, atazanavir, clarithromycin, delavirdine, diltiazem, erythromycin, indinavir, itraconazole, ketoconazole, miconazole, nefazodone, nelfinavir, ritonavir, saquinavir, telithromycin, troleandomycin, verapamil, voriconazole, and grapefruit or grapefruit juice 13. Use of drugs that are known potent CYP3A4 inducers, including but not limited to carbamazepine, phenobarbital, phenytoin, rifabutin,, rifampin, rifapentine, tipranavir, ritonavir, and St. John s wort. 14. Use of drugs that are CYP3A4 substrates with narrow therapeutic indices, including but not limited aripiprazole, ergotamine, halofantrine, pimozide, triazolam, astemizole*, cisapride*, and terfenadine* (* withdrawn from U.S. market) 15. Prior malignancy (other than current NSCLC): patients will not be eligible if they have evidence of active malignancy (other than non-melanoma skin cancer or in situ cervical cancer, or localized and presumed cured prostate cancer with PSA < ULN) within the last 5 years 16. Other severe acute or chronic medical or psychiatric conditions, or laboratory abnormalities that would impart, in the judgment of the investigator and/or sponsor, excess risk associated with study participation or study drug administration, and which would, therefore, make the patient inappropriate for entry into this study.

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified