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Phase I/II Study of S-1, Cisplatin and Docetaxel in Patients with Advanced Gastric Cancer

Phase 1
Conditions
untreated advanced or recurrent gastric cancer
Registration Number
JPRN-UMIN000000484
Lead Sponsor
Department of Gastroenterology and Hematology, Faculty of Medicine, University of Toyama
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
40
Inclusion Criteria

Not provided

Exclusion Criteria

1) Active other malignancy 2) Interstitial pneumonitis, pulmonary fibrosis 3) Massive pleural effusion or massive ascites 4) Active infection 5) Watery diarrhea 6) Other uncontrolled severe illness 7) Brain metastases 8) Pregnant or lactating women 9) Not appropriate for the study at the physician's assessment

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Phase I: Maximum Tolerated Dose, Recommended dose Phase II: Response rate
Secondary Outcome Measures
NameTimeMethod
Toxicity, Progression free survival, Overall survival
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