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Phase II clinical study of nab-PTX/CBDCA (administer 3-weeks on / 1-week off) for patients with clinical stage IIIB/IV or recurrent NSCLC

Phase 2
Conditions
lung cancer
Registration Number
JPRN-UMIN000016255
Lead Sponsor
Shiga University of Medical Science
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
5
Inclusion Criteria

Not provided

Exclusion Criteria

1.With severe myelosuppression. 2.With the history of hypersensitivity for nab-paclitaxel or CBDCA. 3.With active double cancer. 4.With active infectious disease:temperature=>38 5.With clinically important complications. 6.Interstitial pneumonia or pulmonary fibrosis on chest X-rays. 7.Pregnant females, possibly pregnant females, females wishing to become pregnant and nursing mothers. Males that are currently attempting to produce a pregnancy. 8.Accepted continuous use of steroid. 9.Physician concludes that the patient's participation in this trial is inappropriate.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
response rate
Secondary Outcome Measures
NameTimeMethod
progression free survival/overall survival/disease control rate/adverse events/completion rate of treatment
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