A Phase II Study of Irinotecan, Oxaliplatin, Plus TS-1 in Untreated Metastatic Gastric Cancer
- Sponsor
- National Cancer Center, Korea
- Study ID
- NCT00512681
- Phase
- PHASE2
- Status
- Completed
Conditions
- Stomach Neoplasms
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Irinotecan, Oxaliplatin, TS-1 — DRUG* S-1 40 mg/m2/day every 12-h p.o. on days 1(evening)-15 (morning) * Irinotecan 150 mg/m2 mixed in d5w 500 ml iv over 90-min on days 1 * Oxaliplatin 85 mg/m2 mixed in d5w 250 ml iv over 2-h on days 1
Study Details
Patients will be treated with irinotecan (150mg/m2) followed by oxaliplatin (85mg/m2)on day 1 and S-1(80mg/m2/day) from day 1 to 14 every 3 weeks. Patients will receive up to a planned treatment of maximum 12 cycles of chemotherapy. Response assessement will be performed every 2 cycles of chemotherapy.
Key Dates
- Start date
- Jul 31, 2007
- Status verified
- Sep 2009
- Primary completion
- Jul 31, 2009
- Completion
- Jul 31, 2009
Study Design
- Enrollment
- 44 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Primary Outcome Measure
Maximal overall response rate [ Time Frame: During chemotherapy ]
Related Studies
- Tissue Procurement and Natural History Study of Patients With Malignant MesotheliomaRecruiting · National Cancer Institute (NCI) · Bethesda, Maryland
- A Study of Sigvotatug Vedotin in Advanced Solid TumorsPHASE1 · Recruiting · Seagen, a wholly owned subsidiary of Pfizer · Anchorage, Alaska
- A Study of SGN-CEACAM5C in Adults With Advanced Solid TumorsPHASE1 · Recruiting · Seagen, a wholly owned subsidiary of Pfizer · Phoenix, Arizona
- A Study of Disitamab Vedotin With Other Anticancer Drugs in Solid TumorsPHASE2 · Recruiting · Seagen, a wholly owned subsidiary of Pfizer · Tucson, Arizona