MedPath

A Phase II study of Ramucirumab beyond disease progression in combination with Irinotecan after failure of weekly Paclitaxel plus Ramucirumab in advanced gastric cancer patients previously treated with fluoropyrimidine and platinum

Not Applicable
Conditions
Gastric cancer
Registration Number
JPRN-UMIN000022956
Lead Sponsor
The University of Tokyo
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
53
Inclusion Criteria

Not provided

Exclusion Criteria

1)with active double cancers excluding carcinoma in situ 2)with pleural fluid, ascites or pericardial effusion that requires drainage 3)with ileus or constipation (>=grade 3) 4)with a histroy of uncontrollable hypertension or acute coronary syndrome in 6 months 5)with active gastrointestinal bleeding in 14 days 6)with severe or uncotrollable complications such as diabetes mellitus, bowel obstruction, jaundice, liver dysfunction, psychological illness and severe infectious disease. 7)with active hepatitis B or C 8)with HIV infection 9)with a history of interstitial pneumonia, pulmonary fibrosis or irradiation pneumonitis 10)with hemorrhagic diathesis or blood coagulation disorder 11)within 28 days after open abdominal or chest surgery or with unrecoverd surgical wounds 12)pregnant and/or nursing women or men who wish to have children in future 13)judged to be unfit to participate in this study by investigater

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Progression free survival
Secondary Outcome Measures
NameTimeMethod
Achievement ratio of second registration Treatment continuation rate at eight weeks after second registration Response rate Overall survival Safety Quality of life
© Copyright 2025. All Rights Reserved by MedPath