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Clinical Trials/JPRN-UMIN000009993
JPRN-UMIN000009993
Completed
Phase 1

Phase I study on the feasibility of Nedaplatin plus S-1 combination therapy for squamous cell lung cancer. - Nedaplatin plus S-1 combination therapy for squamous cell lung cancer

Fukuoka University Hospital0 sites18 target enrollmentFebruary 18, 2013

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Fukuoka University Hospital
Enrollment
18
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Because of shortage of case accumulation, the study was terminated.

Registry
who.int
Start Date
February 18, 2013
End Date
March 31, 2017
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\. Patient who have severe infection 2\. Pregnant or lactating women. 3\. Multiple cancer 4\. A known history of allergy 5\. A known history of GI bleeding 6\. Patient who have interstitial pneumonia 7\. Patient who have severe diabetes mellitus, liver cirrhosis, renal dysfunction, angina pectoris, arrhythmia, or myocardiac infarction before 3 months 8\. Patient who have therapeutic need of pleural effusion, pericardiac effusion, or SVC syndrome 9\. Patient who have obscure symptoms of brain metastasis. 10\. Patient who have obscure symptoms of peripheral nerve dysfunction 11\. Patient who take flucytosin.of brain 12\. Patient who have severe 13\.patient who is judged as an inappropriate case by the doctor in charge

Outcomes

Primary Outcomes

Not specified

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