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
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.
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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