The purpose of this study is to learn if vinflunine can shrink or slow the growth of cancer in patients with advanced or metastatic stomach cancer who have progressed on a prior treatment with a fluoropyrimidine or taxane-containing chemotherapy regimen. The safety of this treatment will also be studied.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
55
solution for injection, IV, 280/320 mg/m2, every 3 wks, variable duration
Local Institution
Kampung Baharu Nilai, Negeri Sembilan, Malaysia
Local Institution
Quezon City, Philippines
Local Institution
Suwon, Gyeonggi-do, South Korea
Local Institution
Gyeonggi-do, South Korea
The Response Rate (RR: Complete Response [CR]+Partial Response [PR], as defined by Response Evaluation Criteria in Solid Tumors [RECIST]
Time frame: throughout the study
Estimation of the progression free survival and overall survival
Time frame: At the end of the study
The estimation of the disease control rate
Time frame: At the end of the study
The time to response and the duration of response
Time frame: At the end of the study
The evaluation of the safety profile of vinflunine
Time frame: At the end of the study
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Local Institution
Seoul, South Korea
Local Institution
Seoul, South Korea