32 Sites
Multiple Locations, Japan
NCT Number: NCT01207011
The study is to evaluate the effect of amrubicin (AMR) compared to docetaxel (DOC) in the treatment of non-small cell lung cancer (NSCLC).
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Notify Me20 year–74 year
All sexes
Interventional
Phase 3
Multiple Locations, Japan
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
AMR was administered i.v. by 35mg/m2 at day 1, 2 and 3 followed by 3 week rest as 1 course.
DOC was administered i.v. by 60mg/m2 at day 1 followed by 3 week rest as 1 course.
Time frame: 3.3 months
Time frame: 12 months
Time frame: 3 months
Time frame: 4 months
Sumitomo Pharma Co., Ltd.
Industry
A Randomised, Open-Label Phase 3 Trial Comparing Amrubicin Versus Docetaxel in Patients With Non-Small Cell Lung Cancer After Failure of First-Line Chemotherapy
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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