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A Phase I Study of TS-1 in Combination with ABI-007 every three weeks in Patients with Unresectable or Recurrent Gastric Cancer

Phase 1
Conditions
nresectable or Recurrent gastric cancer
Registration Number
JPRN-jRCT2080221526
Lead Sponsor
Taiho Pharmaceutical Co., Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Sex
All
Target Recruitment
30
Inclusion Criteria

Signed, written informed consent.
- Patient has a histologically or cytologically confirmed gastric adenocarcinoma. Or patient has a clinically confirmed unresectable or recurrent gastric cancer.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

Exclusion Criteria

- Patient who is contraindicated to TS-1 or Paclitaxel.(Refer to Package Insert).
- Patient has multiple cancer.
- Patient has a clinically significant medical history or disease complication.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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