Lung Cancer Clinical Trial

BI 2536 Second Line Monotherapy in SCLC

Summary

Open label, uncontrolled Phase II trial to assess the efficacy and safety of BI 2536 in second line treatment in sensitive-relapse SCLC patients.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Patients with histologically or cytologically confirmed, -sensitive-relapse- SCLC defined by a relapse 60 days or more after cessation of prior first-line chemotherapy.
Patients with at least one measurable lesion, with longest diameter to be recorded as 20 mm or greater.
Life expectancy of at least three months and ECOG performance score of 2 or less and written informed consent that must be consistent with ICH-GCP Guidelines.

Exclusion Criteria:

More than one prior regimen of chemotherapy, mixed small cell/large cell or combined small cell histology.
Symptomatic brain metastases or leptomeningeal disease
Patients with ascites, patients who have any other life-threatening illness or organ system dysfunction, or other malignancies diagnosed within the past five (5) years (other than non melanomatous skin cancer)
Absolute neutrophil count (ANC) <1,500/µl, platelet count <100,000/µl, or hemoglobin <9 mg/dl
Total bilirubin >1.5 x ULN, aspartame amino transferase (AST) and/or alanine amino transferase (ALT) >2.5 x ULN, or aspartate amino transferase (AST) and/or alanine amino transferase (ALT) >5 x ULN in case of known liver metastases, serum creatinine >2.0 mg/dl (>176 µmol/L, SI Unit equivalent)
Chemo-, hormone- (other than Megace®) or immunotherapy within the past 4 weeks or within less than 4 half-life times of the previous drug prior to treatment with the trial drug
Radiation therapy within the past 2 weeks prior to or during treatment with the trial drug
Patients with any serious active infection (i.e., requiring an IV antibiotic, antifungal, or antiviral agents), patients with known HIV, hepatitis-B or -C infection
Known or suspected active drug or alcohol abuse
Treatment with any other investigational drug within the past 4 weeks or within less than 4 half-life times of the investigational drug
Patients with a known pre-existing coagulopathy or requiring therapeutic anticoagulation with warfarin (Coumadin ®)
Patients with neuropathy (sensory or motor) CTCAE 3

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

23

Study ID:

NCT00412880

Recruitment Status:

Completed

Sponsor:

Boehringer Ingelheim

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There is 1 Location for this study

See Locations Near You

1216.11.007 Boehringer Ingelheim Investigational Site
Fayetteville Arkansas, , United States
1216.11.003 Boehringer Ingelheim Investigational Site
Chicago Illinois, , United States
1216.11.006 Boehringer Ingelheim Investigational Site
Evanston Illinois, , United States
1216.11.002 Boehringer Ingelheim Investigational Site
Boston Massachusetts, , United States
1216.11.005 Boehringer Ingelheim Investigational Site
Saint Louis Missouri, , United States
1216.11.001 Boehringer Ingelheim Investigational Site
Chapel Hill North Carolina, , United States
1216.11.011 Boehringer Ingelheim Investigational Site
Charleston South Carolina, , United States
1216.11.010 Boehringer Ingelheim Investigational Site
Greenville South Carolina, , United States
1216.11.012 Boehringer Ingelheim Investigational Site
Seattle Washington, , United States
1216.11.009 Alberta Cancer Board
Edmonton Alberta, , Canada

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

23

Study ID:

NCT00412880

Recruitment Status:

Completed

Sponsor:


Boehringer Ingelheim

How clear is this clinincal trial information?

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