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A Phase 3, Double-Blind, Placebo-Controlled Study of Maintenance Pemetrexed Plus Best Supportive Care Versus Best Supportive Care Immediately Following Induction Treatment With Pemetrexed + Cisplatin for Advanced Non-squamous Non-Small Cell Lung Cancer.


Phase 3
18 Years
N/A
Open (Enrolling)
Both
Non-Small Cell Lung Cancer

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Trial Information

A Phase 3, Double-Blind, Placebo-Controlled Study of Maintenance Pemetrexed Plus Best Supportive Care Versus Best Supportive Care Immediately Following Induction Treatment With Pemetrexed + Cisplatin for Advanced Non-squamous Non-Small Cell Lung Cancer.

Inclusion Criteria


Inclusion Criteria for the Induction Phase:

- You must sign an informed consent document for clinical research.

- You must have Stage IIIB or IV nonsquamous Non-Small Cell Lung Cancer.

- You must at least be able to be physically mobile, take care of yourself, and must be
up and about and able to perform light activities such as light housework or office
work.

- You are allowed to have had prior radiation therapy as long as it was not to more
than 25% of the bone marrow and did not include the whole pelvis. Thoracic radiation
must be completed more than 30 days before the study. You must be recovered from the
toxic effects (except hair loss).

- You must have at least 1 measurable tumor lesion according to the Response Evaluation
Criteria in Solid Tumors (RECIST) guidelines or disease that can be evaluated by
computed tomography (CT) Scan.

- Your test results assessing the function of your blood forming tissue, kidneys, and
liver must be satisfactory.

- You must be 18 years of age or older.

- Women must be sterile, postmenopausal or on contraception and men must be on
contraception or sterile (e.g. post-vasectomy).

Exclusion Criteria for the Induction Phase:

- You cannot have squamous cell and/or mixed small cell, non-small cell lung cancer

- You cannot have received other investigational drugs within the last 30 days of
entering the trial.

- You cannot have previously completed or withdrawn from this study or any other study
investigating pemetrexed.

- You cannot have other serious on-going illnesses including active infections.

- You cannot have a serious cardiac condition, such as a heart attack, angina, or heart
disease within 6 months of entering the trial.

- You cannot have had another form of cancer other than superficial basal cell and
superficial squamous (skin) cell cancer, or carcinoma in situ of the cervix within
the last 5 years. Patients with a history of low-grade (Gleason score less than or
equal to 6) localized prostate cancer will be eligible even if diagnosed less than 5
years ago.

- You cannot have known central nervous system (CNS) metastases, other than treated,
stable brain metastasis.

- You cannot be receiving nor have received any prior systemic anticancer therapy for
lung cancer (including chemotherapy given after surgery in early-stage treatment).

- 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 received a recent (within 30 days) or are receiving a yellow fever
vaccination.

- You are unable to stop taking more than 1.3 grams of aspirin on a daily basis or
other non-steroidal anti-inflammatory drugs (NSAIDs).

- You are unable or unwilling to take folic acid, injections of vitamin B12, or
corticosteroids.

- You cannot be pregnant or breastfeeding.

Inclusion criteria at Randomization for the Maintenance Phase:

- You must at least be able to be physically mobile, take care of yourself, and must be
up and about and able to perform light activities such as light housework or office
work.

- You must have documented radiographic evidence of a tumor response of complete
response (CR), partial response (PR), or stable disease (SD) according to the
Response Evaluation Criteria in Solid Tumors (RECIST) guidelines. Tumor assessment
must occur between Cycle 4 (Day 1) of induction therapy and the date of
randomization. This response does not have to be confirmed in order for the patient
to be randomized to the maintenance phase.

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Outcome Measure:

Investigator-assessed Objective Progression-free Survival (PFS)

Outcome Description:

Investigator-assessed objective PFS was measured from the date of randomization to the first date of objectively determined progressive disease (PD) or death from any cause. For patients not known to have died as of the data cutoff date and who did not have objective PD, PFS was censored at the date of last objective tumor assessment. PD was determined using Response Evaluation Criteria In Solid Tumors (RECIST) criteria. PD = 20% increase in sum of longest diameter of target lesions.

Outcome Time Frame:

Date of randomization to the date of measured PD or date of death from any cause (up to 19.3 months)

Safety Issue:

Yes

Principal Investigator

Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)

Investigator Role:

Study Director

Investigator Affiliation:

Eli Lilly and Company

Authority:

United States: Food and Drug Administration

Study ID:

12560

NCT ID:

NCT00789373

Start Date:

November 2008

Completion Date:

September 2013

Related Keywords:

  • Non-Small Cell Lung Cancer
  • Carcinoma, Non-Small-Cell Lung
  • Lung Neoplasms

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