Lung Cancer Clinical Trial

A Randomized Phase 2 Study of Ixabepilone Plus Carboplatin and Paclitaxel Plus Carboplatin in Advanced Nonsmall-Cell Lung Cancer

Summary

The purpose of this study is to determine whether progression-free survival with ixabepilone is superior to that achieved with paclitaxel plus carboplatin in participants with advanced nonsmall-cell lung cancer and beta III (βIII)-tubulin-positive tumors.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Histologically confirmed non-small cell lung cancer (NSCLC)(squamous cell, adenocarcinoma, large cell, or bronchoalveolar carcinoma)
Stage IIIB NSCLC with pleural effusion, Stage IV NSCLC, or recurrent disease following surgery with or without radiation therapy
Available paraffin-embedded tissue to measure the expression levels of βIII tubulin
Disease measurable by Response Evaluation Criteria in Solid Tumors, with at least 1 target lesion situated outside any previous radiotherapy field
Karnofsky performance status of 70-100
Life expectancy of at least 3 months
Men and women, ages 18 years and older

Exclusion Criteria:

Uncontrolled brain metastases
Peripheral neuropathy greater than Grade 1
Fewer than 4 weeks from prior radiation therapy or locoregional surgeries to randomization date (less than 1 week from focal/palliative radiotherapy or minor surgery)
Any concurrent malignancy other than nonmelanoma skin cancer or carcinoma in situ of the cervix
Known HIV-positive status
Absolute neutrophil count lower than 1500 cells mm^3
Total bilirubin level higher than upper limit of normal (ULN) as defined by the institution (with the exception of elevation due to Gilbert's syndrome)
Aspartate transaminase or alanine transaminase level higher than 2.5*ULN
Serum creatine level of 1.5 mg/dL or higher
Renal function with a creatinine clearance of less than 50 mL/min (as calculated with the Cockcroft and Gault equation)
Any prior antineoplastic systemic regimens.

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

260

Study ID:

NCT00723957

Recruitment Status:

Completed

Sponsor:

R-Pharm

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There are 33 Locations for this study

See Locations Near You

Scripps Cancer Center
La Jolla California, 90237, United States
Uof Md,Greenebaum Cancer Ctr.
Baltimore Maryland, 21201, United States
Local Institution
Capital Federal Buenos Aires, 1425, Argentina
Local Institution
Capital Federal Buenos Aires, 1437, Argentina
Local Institution
Buenos Aires , C1426, Argentina
Local Institution
Bankstown New South Wales, 2200, Australia
Local Institution
Frankston Victoria, 3199, Australia
Local Institution
Nedlands Western Australia, 6009, Australia
Local Institution
Poitiers , 86021, France
Local Institution
Strasbourg , 67085, France
Local Institution
Strasbourg , 67090, France
Local Institution
Bad Berka , 99437, Germany
Local Institution
Grosshansdorf , 22927, Germany
Local Institution
Ulm , 89081, Germany
Local Institution
Genova , 16132, Italy
Local Institution
Milano , 20133, Italy
Local Institution
Sondrio , 23100, Italy
Local Institution
Terni , 05100, Italy
Local Institution
Goyang-Si Gyeonggi-Do, 411-7, Korea, Republic of
Local Institution
Seoul , 120-7, Korea, Republic of
Local Institution
Seoul , 135-7, Korea, Republic of
Local Institution
Seoul , 138-7, Korea, Republic of
Local Institution
Chelyabinsk , 45408, Russian Federation
Local Institution
Kazan , 42002, Russian Federation
Local Institution
Moscow , 115 4, Russian Federation
Local Institution
Moscow , 12912, Russian Federation
Local Institution
Ryazan , 39001, Russian Federation
Local Institution
St. Petersburg , 19429, Russian Federation
Local Institution
St. Petersburg , 19825, Russian Federation
Local Institution
Baracaldo (Vizcaya) , 48903, Spain
Local Institution
Taichung , 407.5, Taiwan
Local Institution
Taipei , 112, Taiwan
Local Institution
Taoyuan Hsien , 333, Taiwan

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

260

Study ID:

NCT00723957

Recruitment Status:

Completed

Sponsor:


R-Pharm

How clear is this clinincal trial information?

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