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Phase I study of nedaplatin and S-1 in patients with advanced or relapsed squamous cell lung cancer

Not Applicable
Conditions
Squamous cell lung cancer
Registration Number
JPRN-UMIN000036387
Lead Sponsor
Kagawa University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
9
Inclusion Criteria

Not provided

Exclusion Criteria

1)Severe complication 2)interstitial penumonia 3)positive for HBs antigen 4)Pleural effusion, ascites, or pericardial effusion which need drainage 5)double malignancy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
determination of maximum dose and estimation of recommendation dose
Secondary Outcome Measures
NameTimeMethod
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