A Study of Pemetrexed, Carboplatin and Bevacizumab in Patients With Nonsquamous Non-Small Cell Lung Cancer

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
Eli Lilly and Company
ClinicalTrials.gov Identifier:
NCT00762034
First received: September 26, 2008
Last updated: August 29, 2014
Last verified: August 2014
  Purpose

This study will compare overall survival in patients with Stage IIIB or IV nonsquamous non-small cell lung cancer.


Condition Intervention Phase
Non-small Cell Lung Cancer
Drug: Pemetrexed
Drug: Paclitaxel
Drug: Carboplatin
Biological: Bevacizumab
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Randomized, Open-Label, Phase 3 Study of Pemetrexed Plus Carboplatin and Bevacizumab Followed by Maintenance Pemetrexed and Bevacizumab Versus Paclitaxel Plus Carboplatin and Bevacizumab Followed by Maintenance Bevacizumab in Patients With Stage IIIB or IV Nonsquamous Non-Small Cell Lung Cancer

Resource links provided by NLM:


Further study details as provided by Eli Lilly and Company:

Primary Outcome Measures:
  • Overall Survival [ Time Frame: Baseline to date of death from any cause (up to 37.06 months) ] [ Designated as safety issue: No ]
    Overall survival (OS) is the duration from date of randomization to date of death from any cause. Participants were censored at the date they were last known to be alive.


Secondary Outcome Measures:
  • Percentage of Participants With a Complete Response (CR) and Partial Response (PR) (Overall Response Rate) [ Time Frame: Baseline to measured progressive disease (up to 37.06 months) ] [ Designated as safety issue: No ]
    Overall Response Rate (ORR) is the number of participants with a Complete Response (CR) and Partial Response (PR) divided by the total number of randomized participants per arm, then multiplied by 100. Response is based on the Response Evaluation Criteria In Solid Tumors (RECIST 1.0) criteria. Complete Response (CR) was defined as the disappearance of all target lesions. Partial Response (PR) was defined as at least a 30% decrease in sum of longest diameter of target lesions compared to baseline or the complete disappearance of target lesions, with persistence of 1 or more nontarget lesion(s) and no new lesions.

  • Percentage of Participants With a Complete Response (CR), Partial Response (PR), and Stable Disease (SD) (Disease Control Rate) [ Time Frame: Baseline to measured progressive disease (up to 37.06 months) ] [ Designated as safety issue: No ]
    Disease Control Rate (DCR) is the number of participants with a Complete Response (CR), Partial Response (PR), and Stable Disease (SD) divided by the total number of randomized participants per arm, then multiplied by 100. Response is based on the Response Evaluation Criteria In Solid Tumors (RECIST 1.0) criteria. Complete Response (CR) was defined as the disappearance of all target lesions. Partial Response (PR) was defined as at least a 30% decrease in sum of longest diameter of target lesions compared with baseline or the complete disappearance of target lesions, with persistence of 1 or more nontarget lesion(s) and no new lesions. Progressive Disease (PD) was defined as at least 20% increase in sum of longest diameter of target lesions compared with the smallest sum of the longest diameter recorded since the start of treatment or the appearance of 1 or more new lesion(s). Stable Disease (SD) was defined as small changes that did not meet above criteria.

  • Progression Free Survival Time [ Time Frame: Baseline to measured progressive disease or date of death from any cause (up to 33.54 months) ] [ Designated as safety issue: No ]
    Progression free survival (PFS) is defined as the time from date of randomization to the date of objective disease progression or death due to any cause. Participants were censored at date of last PFS assessment prior to the cutoff date or the date of initiation of subsequent systemic anticancer therapy, whichever was earlier.

  • Time to Progressive Disease [ Time Frame: Baseline to measured progressive disease (up to 37.06 months) ] [ Designated as safety issue: No ]
    Time to progressive disease was defined as the time from randomization to the first date of objective disease progression. Participants were censored at date of last PFS assessment prior to the cutoff date or the date of initiation of subsequent systemic anticancer therapy, whichever was earlier.

  • Safety and Toxicity Profile of Study Treatments [ Time Frame: Baseline to study endpoint (up to 37.06 months) ] [ Designated as safety issue: Yes ]
    Safety and toxicity profile was defined as serious and other non-serious adverse events. A summary of serious and all other non-serious adverse events is located in the Reported Adverse Event module.

  • Duration of Hospitalizations Per Participant [ Time Frame: Baseline to study endpoint (up to 37.06 months) ] [ Designated as safety issue: Yes ]
    Length of hospitalization in participants hospitalized during the study or within 30 days of discontinuation regardless of whether the hospitalization was or was not due to study drug.

  • Number of Participants Who Received a Transfusion [ Time Frame: Baseline to study endpoint (up to 37.06 months) ] [ Designated as safety issue: Yes ]
  • Number of Participants Receiving Concomitant Medication [ Time Frame: Baseline to study endpoint (up to 37.06 months) ] [ Designated as safety issue: Yes ]
  • Change From Baseline in Participant Reported Outcomes as Assessed by the Functional Assessment of Cancer Therapy - General (FACT-G) [ Time Frame: Baseline, up to first 10 cycles (4 induction and 6 maintenance cycles, cycle=21 days) ] [ Designated as safety issue: Yes ]
    The FACT-G is a validated instrument used to measure quality of life (QOL) in participants with cancer consisting of the 27-item questionnaire and is organized into subscales, each designed to assess a QOL domain: physical well-being (PWB)-7 items; social/family well-being (SWB)-7 items; emotional well-being (EWB)-6 items; functional well-being (FWB)-7 items. Each item uses a 5 point rating scale (0="not at all" and 4=equals "very much"). FACT-G Total is the sum of the scores of all 4 subscales and ranges from 0 to 108. Higher scores indicate better QOL. Least squares mean (LSmean) change is calculated using the linear-mixed model (LMM) analysis controlled for treatment, baseline value, time point and treatment by time point interaction.

  • Change From Baseline in Participant Reported Outcomes as Assessed by the Functional Assessment of Cancer Therapy - Lung (FACT-L) [ Time Frame: Baseline, up to first 10 cycles (4 induction and 6 maintenance cycles, cycle=21 days) ] [ Designated as safety issue: Yes ]
    FACT-L is a valid instrument used to measure quality of life (QOL) in participants with cancer consisting of the 27-item FACT-General (G) and 9-item lung cancer subscale (LCS). FACT-G is organized into subscales: physical well-being (PWB)-7 items; social/family well-being (SWB)-7 items; emotional well-being (EWB)-6 items; functional well-being (FWB)-7 items. Each item uses a 5 point rating scale (0="not at all" and 4=equals "very much"). FACT-L Total Score=4 subscales + LCS and ranges from 0 to 144. Trial Outcome Index-Lung (TOI-L)=PWB+FWB+LCS and ranges from 0 to 92. Higher scores indicate better QOL. Least squares mean (LSmean) change is calculated using the linear-mixed model (LMM) analysis controlled for treatment, baseline value, time point and treatment by time point interaction.

  • Change From Baseline in Participant Reported Outcomes as Assessed by the Functional Assessment of Cancer Therapy/Gynecologic Oncology Group- Neurotoxicity (FACT/GOG-Ntx) [ Time Frame: Baseline, up to first 10 cycles (4 induction and 6 maintenance cycles, cycle=21 days) ] [ Designated as safety issue: Yes ]
    FACT/GOG-Ntx is a validated instrument used to measure quality of life (QOL) in participants with cancer and neurotoxicity (Ntx) consisting of 27-item FACT-General (G) and 11-item Ntx subscale. FACT-G is organized into domain subscales: physical well-being (PWB)-7 items; social/family well-being (SWB)-7 items; emotional well-being (EWB)-6 items; functional well-being (FWB)-7 items; each uses a 5 point rating scale (0="not at all" and 4=equals "very much"). FACT/GOG-Ntx Total Score=sum 5 subscales and ranges from 0-152. Ntx Trial Outcome Index (TOI-Ntx)=PWB+FWB+NTX and range from 0-100. For all FACT scales, higher scores indicate better QOL. Least squares mean (LSmean) change is calculated using the linear-mixed model (LMM) analysis controlled for treatment, baseline value, time point and treatment by time point interaction.

  • Pharmacokinetics (PK): Maximum Observed Drug Concentration (Cmax) for Pemetrexed [ Time Frame: Cycle 1 (pre-dose, 0.17, 0.33, 0.58, 0.83, 1, 1.75, 2.5, 4. 6. 8, and 24 hours post-dose) ] [ Designated as safety issue: No ]
  • Pharmacokinetics (PK): Elimination Half-life (t1/2) for Pemetrexed [ Time Frame: Cycle 1 (pre-dose, 0.17, 0.33, 0.58, 0.83, 1, 1.75, 2.5, 4. 6. 8, and 24 hours post-dose) ] [ Designated as safety issue: No ]
  • Pharmacokinetics (PK): Area Under the Concentration Time Curve From Zero to Infinity (AUC(0-∞)) for Pemetrexed [ Time Frame: Cycle 1 (pre-dose, 0.17, 0.33, 0.58, 0.83, 1, 1.75, 2.5, 4. 6. 8, and 24 hours post-dose) ] [ Designated as safety issue: No ]
  • Pharmacokinetics (PK): Pemetrexed Clearance (CL) [ Time Frame: Cycle 1 (pre-dose, 0.17, 0.33, 0.58, 0.83, 1, 1.75, 2.5, 4. 6. 8, and 24 hours post-dose) ] [ Designated as safety issue: No ]
  • Pharmacokinetics (PK): Maximum Observed Drug Concentration (Cmax) for Total (Bound and Unbound) Platinum and Unbound Platinum [ Time Frame: Cycle 1 (pre-dose, 0.25, 0.5, 0.67, 1.42, 2.17, 4, 6, 8, 24, 48, and 72 hours post-dose) ] [ Designated as safety issue: No ]
    Platinum is a metabolite of Carboplatin (Carbo) and is found in the blood as both a bound and unbound form.

  • Pharmacokinetics (PK): Elimination Half-life (t1/2) for Total (Bound and Unbound) Platinum and Unbound Platinum [ Time Frame: Cycle 1 (pre-dose, 0.25, 0.5, 0.67, 1.42, 2.17, 4, 6, 8, 24, 48, and 72 hours post-dose) ] [ Designated as safety issue: No ]
    Platinum is a metabolite of Carboplatin (Carbo) and is found in the blood as both a bound and unbound form.

  • Pharmacokinetics (PK): Area Under the Concentration Time Curve From Zero to Infinity (AUC(0-∞)) for Total (Bound and Unbound) Platinum and Unbound Platinum [ Time Frame: Cycle 1 (pre-dose, 0.25, 0.5, 0.67, 1.42, 2.17, 4, 6, 8, 24, 48, and 72 hours post-dose) ] [ Designated as safety issue: No ]
    Platinum is a metabolite of Carboplatin (Carbo) and is found in the blood as both a bound and unbound form.

  • Pharmacokinetics (PK): Platinum Clearance (CL) for Total (Bound and Unbound) and Unbound Forms [ Time Frame: Cycle 1 (pre-dose, 0.25, 0.5, 0.67, 1.42, 2.17, 4, 6, 8, 24, 48, and 72 hours post-dose) ] [ Designated as safety issue: No ]
    Platinum is a metabolite of Carboplatin (Carbo) and is found in the blood as both a bound and unbound form.

  • Pharmacokinetics (PK): Maximum Observed Drug Concentration (Cmax) for Bevacizumab [ Time Frame: Cycle 1 (pre-dose, 0.75, 1.5, 3, 5, 7, 24, 48, 72, 168, 336, and 503 hours post-dose) ] [ Designated as safety issue: No ]
  • Pharmacokinetics (PK): Elimination Half-life (t1/2) for Bevacizumab [ Time Frame: Cycle 1 (pre-dose, 0.75, 1.5, 3, 5, 7, 24, 48, 72, 168, 336, and 503 hours post-dose) ] [ Designated as safety issue: No ]
  • Pharmacokinetics (PK): Area Under the Concentration Time Curve From Zero to Infinity (AUC(0-∞)) Bevacizumab [ Time Frame: Cycle 1 (pre-dose, 0.75, 1.5, 3, 5, 7, 24, 48, 72, 168, 336, and 503 hours post-dose) ] [ Designated as safety issue: No ]
  • Pharmacokinetics (PK): Bevacizumab Clearance (CL) [ Time Frame: Cycle 1 (pre-dose, 0.75, 1.5, 3, 5, 7, 24, 48, 72, 168, 336, and 503 hours post-dose) ] [ Designated as safety issue: No ]
  • Translational Research: Number of Participants With Epidermal Growth Factor Receptor (EGFR) Mutations [ Time Frame: Baseline ] [ Designated as safety issue: No ]
    Epidermal Growth Factor Receptor (EGFR) mutations were measured by polymerase chain reaction (PCR).

  • Translational Research: Overall Survival (OS) Based on Nuclear Thyroid Transcription Factor-1 (TTF-1) Expression Regardless of Study Treatment [ Time Frame: Baseline to date of death from any cause (up to 37.06 months) ] [ Designated as safety issue: No ]
    Nuclear Thyroid Transcription Factor-1 (TTF-1) expression was measured using an Immunohistochemistry (IHC) assay which were scored using a 0 (negative, no staining) to 3+ (brightest staining) scoring system, and H score is a calculated using formula: 1x(percentage of cells stained 1+) + 2x(percentage of cells stained 2+) + 3x(percentage of cells stained 3+). TTF-1 Positive have an H score >0 and TTF-1 Negative have an H score=0. Overall survival (OS) is the duration from date of randomization to date of death from any cause. Participants were censored at the date they were last known to be alive.

  • Translational Research: Overall Survival (OS) Based on Cytoplasmic and Nuclear Thymidylate Synthase (TS) Expression [ Time Frame: Baseline to date of death from any cause (up to 37.06 months) ] [ Designated as safety issue: No ]
    Cytoplasmic and nuclear Thymidylate Synthase (TS) expression was measured using an Immunohistochemistry (IHC) assay which were scored using a 0 (negative, no staining) to 3+ (brightest staining) scoring system for cytoplasmic and nuclear staining, and H score was calculated using formula: 1x(percentage of cells stained 1+) + 2x(percentage of cells stained 2+) + 3x(percentage of cells stained 3+). TS Positive have an H score >0 and TS Negative have an H score=0. Overall survival (OS) is the duration from date of randomization to date of death from any cause. Participants were censored at the date they were last known to be alive.

  • Translational Research: Overall Survival (OS) Based on Cytoplasmic and Membrane Folate Receptor Alpha (FR-α) Expression [ Time Frame: Baseline to date of death from any cause (up to 37.06 months) ] [ Designated as safety issue: No ]
    Cytoplasmic and membrane Folate Receptor Alpha (FR-α) expression was measured using an Immunohistochemistry (IHC) assay which were scored using a 0 (negative, no staining) to 3+ (brightest staining) scoring system for cytoplasmic or membrane staining, and H score is a calculated using formula: 1x(percentage of cells stained 1+) + 2x(percentage of cells stained 2+) + 3x(percentage of cells stained 3+). FR-α Positive have an H score >0 and FR-α Negative have an H score=0. Overall survival (OS) is the duration from date of randomization to date of death from any cause. Participants were censored at the date they were last known to be alive.


Enrollment: 939
Study Start Date: December 2008
Estimated Study Completion Date: October 2014
Primary Completion Date: April 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Pem/Carbo/Bev
Pemetrexed (Pem), carboplatin (Carbo) and bevacizumab (Bev) followed by pemetrexed and bevacizumab
Drug: Pemetrexed
Induction therapy 500 milligram per meter squared (mg/m^2) intravenously (IV) every 21 days (with carboplatin and bevacizumab) for up to 4 cycles of 21 days
Other Names:
  • Alimta
  • LY231514
Drug: Pemetrexed
Maintenance therapy 500 mg/m^2 IV every 21 days (with bevacizumab) until progressive disease or treatment discontinuation
Other Names:
  • Alimta
  • LY231514
Drug: Carboplatin
Induction therapy area under the concentration curve (AUC) 6 IV every 21 days for up to 4 cycles of 21 days
Biological: Bevacizumab
Induction therapy 15 milligrams per kilogram (mg/kg) IV every 21 days for up to 4 cycles of 21 days
Biological: Bevacizumab
Maintenance therapy 15 mg/kg IV every 21 days until progressive disease or treatment discontinuation.
Active Comparator: Pac/Carbo/Bev
Paclitaxel (Pac), carboplatin (Carbo) and bevacizumab (Bev) followed by bevacizumab
Drug: Paclitaxel
Induction therapy 200 mg/m^2 IV every 21 days (with carboplatin and bevacizumab) for up to 4 cycles of 21 days
Drug: Carboplatin
Induction therapy area under the concentration curve (AUC) 6 IV every 21 days for up to 4 cycles of 21 days
Biological: Bevacizumab
Induction therapy 15 milligrams per kilogram (mg/kg) IV every 21 days for up to 4 cycles of 21 days
Biological: Bevacizumab
Maintenance therapy 15 mg/kg IV every 21 days until progressive disease or treatment discontinuation.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • You must sign an informed consent document for clinical research.
  • You must have Stage IIIB or Stage IV nonsquamous non-small cell lung cancer.
  • You must not have received any prior treatment for your disease.
  • Prior radiation therapy is allowed to < 25% of the bone marrow; however, prior radiation to the whole pelvis is not allowed. If you have had radiation therapy to the chest, you are not eligible to participate.
  • You must be at least 18 years of age or older.
  • You must have measureable tumor lesions according to the Response Evaluation Criteria in Solid Tumors (RECIST) or disease can be evaluated on computed tomography (CT) scan.
  • Your test results assessing the function of blood forming tissue, kidneys and liver must be satisfactory.
  • Women must be sterile, postmenopausal or on contraception and men must be sterile (for example post-vasectomy) or on contraception.

Exclusion Criteria:

  • You cannot have clinically significant third-space fluid collections (e.g. ascites or pleural effusions that cannot be controlled by drainage or other procedures).
  • You cannot have Non-small Cell Lung Carcinoma (NSCLC) of predominantly squamous cell histology.
  • You cannot have known central nervous system (CNS) disease, other than stable, treated brain metastasis.
  • You cannot have undergone a surgical procedure, open biopsy, open pleurodesis, or significant traumatic injury within 28 days of starting the study treatment, or have an anticipated need for major surgery during the study.
  • You cannot have a history of gastrointestinal fistula, perforation, or abscess, inflammatory bowel disease, or diverticulitis.
  • You are currently receiving ongoing treatment with full-dose warfarin or equivalent.
  • You cannot have significant vascular disease, serious cardiac conditions (such as heart attack), stroke or transient ischemic attack within 6 months of the trial.
  • You cannot have evidence of bleeding diathesis or coagulopathy (in the absence of therapeutic anticoagulation).
  • You cannot have inadequately controlled hypertension, or a history of hypertensive crisis or hypertensive encephalopathy.
  • You cannot have a serious, nonhealing wound, active ulcer, or untreated bone fracture.
  • You cannot have another form of cancer, other than superficial basal cell and superficial squamous (skin) cell, or carcinoma in situ of the cervix within the last 5 years.
  • You cannot have received an investigational treatment within 30 days prior to the trial.
  • You cannot have previously received treatment with paclitaxel, carboplatin, pemetrexed, or bevacizumab.
  • You cannot be pregnant or breast-feeding.
  • You cannot have a known sensitivity to any component of paclitaxel, carboplatin, pemetrexed, or bevacizumab.
  • You cannot have a history of hemoptysis (coughing blood) within 3 months prior to the trial.
  • You are unable to stop taking aspirin more than 1.3 grams per day or other nonsteroidal anti-inflammatory drugs (NSAIDs).
  • You are unable or unwilling to take folic acid or vitamin B12 supplementation.
  • You are unable to take corticosteroids.
  • You have any other on-going illnesses including active infections that may not allow you to adhere to the requirements of the trial.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00762034

  Hide Study Locations
Locations
United States, Arkansas
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Fayetteville, Arkansas, United States, 72703
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Jonesboro, Arkansas, United States, 72401
United States, California
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Alhambra, California, United States, 91801
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Bakersfield, California, United States, 93309
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Duarte, California, United States, 91010
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Fountain Valley, California, United States, 92708
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Fullerton, California, United States, 92835
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La Verne, California, United States, 91750
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Long Beach, California, United States, 90813
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Los Angeles, California, United States, 90095
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Northridge, California, United States, 91325
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Rancho Mirage, California, United States, 92270
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Redondo Beach, California, United States, 90277
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Santa Barbara, California, United States, 93105
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Santa Maria, California, United States, 93454
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Santa Rosa, California, United States, 95403
United States, Colorado
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Grand Junction, Colorado, United States, 81501
United States, Florida
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Boca Raton, Florida, United States, 33486
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Coral Springs, Florida, United States, 33065
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Fort Myers, Florida, United States, 33916
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Jacksonville, Florida, United States, 32256
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Lake Worth, Florida, United States, 33467
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Melbourne, Florida, United States, 32901
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Orlando, Florida, United States, 32804
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Pembroke Pines, Florida, United States, 33028
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Port St Lucie, Florida, United States, 34952
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Stuart, Florida, United States, 34994
United States, Georgia
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Athens, Georgia, United States, 30607
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Augusta, Georgia, United States, 30901
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Fort Gordon, Georgia, United States, 30905
United States, Illinois
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Chicago, Illinois, United States, 60612
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Gurnee, Illinois, United States, 60031
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Skokie, Illinois, United States, 60077
United States, Indiana
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New Albany, Indiana, United States, 47150
United States, Kansas
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Wichita, Kansas, United States, 67214
United States, Kentucky
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Louisville, Kentucky, United States, 40205
United States, Louisiana
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Baton Rouge, Louisiana, United States, 70809
United States, Maryland
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Baltimore, Maryland, United States, 21237
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Bethesda, Maryland, United States, 20817
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Chevy Chase, Maryland, United States, 20815
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Frederick, Maryland, United States, 21701
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Rockville, Maryland, United States, 20850
United States, Massachusetts
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Boston, Massachusetts, United States, 02115
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Framingham, Massachusetts, United States, 01701
United States, Michigan
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Lambertville, Michigan, United States, 48144
United States, Minnesota
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Duluth, Minnesota, United States, 55805
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Minneapolis, Minnesota, United States, 55417
United States, Missouri
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St Louis, Missouri, United States, 63110
United States, Nevada
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Reno, Nevada, United States, 89502
United States, New York
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Bronx, New York, United States, 10467
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Stony Brook, New York, United States, 11794
United States, North Carolina
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Chapel Hill, North Carolina, United States, 27514
United States, Ohio
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Cincinnati, Ohio, United States, 45242
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Columbus, Ohio, United States, 43219
United States, Oklahoma
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Oklahoma City, Oklahoma, United States, 73120
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Tulsa, Oklahoma, United States, 74136
United States, Pennsylvania
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Kittanning, Pennsylvania, United States, 16201
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Willow Grove, Pennsylvania, United States, 19090
United States, South Carolina
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Columbia, South Carolina, United States, 29210
United States, Tennessee
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Knoxville, Tennessee, United States, 37920
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Memphis, Tennessee, United States, 38120
United States, Texas
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San Antonio, Texas, United States, 78229
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The Woodlands, Texas, United States, 77380
United States, Virginia
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Abingdon, Virginia, United States, 24211
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Richmond, Virginia, United States, 23230
United States, Washington
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Tacoma, Washington, United States, 98405
United States, Wisconsin
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Milwaukee, Wisconsin, United States, 53226
Sponsors and Collaborators
Eli Lilly and Company
Investigators
Study Director: Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMC - 5 hours, EST) Eli Lilly and Company
  More Information

No publications provided by Eli Lilly and Company

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Eli Lilly and Company
ClinicalTrials.gov Identifier: NCT00762034     History of Changes
Other Study ID Numbers: 9707, H3E-MC-JMHD
Study First Received: September 26, 2008
Results First Received: March 28, 2013
Last Updated: August 29, 2014
Health Authority: United States: Food and Drug Administration

Additional relevant MeSH terms:
Lung Neoplasms
Carcinoma, Non-Small-Cell Lung
Respiratory Tract Neoplasms
Thoracic Neoplasms
Neoplasms by Site
Neoplasms
Lung Diseases
Respiratory Tract Diseases
Carcinoma, Bronchogenic
Bronchial Neoplasms
Paclitaxel
Bevacizumab
Pemetrexed
Carboplatin
Antineoplastic Agents, Phytogenic
Antineoplastic Agents
Therapeutic Uses
Pharmacologic Actions
Tubulin Modulators
Antimitotic Agents
Mitosis Modulators
Molecular Mechanisms of Pharmacological Action
Angiogenesis Inhibitors
Angiogenesis Modulating Agents
Growth Substances
Physiological Effects of Drugs
Growth Inhibitors
Antimetabolites, Antineoplastic
Antimetabolites
Enzyme Inhibitors

ClinicalTrials.gov processed this record on October 19, 2014