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Clinical pharmacology study to investigate the food effect on pharmacokinetics of TAS-102.

Phase 1
Conditions
Patients with solid tumor
Registration Number
JPRN-jRCT2080221443
Lead Sponsor
Taiho Pharmaceutical Co., Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Sex
All
Target Recruitment
16
Inclusion Criteria

1) Signed, written informed consent.
2) Histologically or cytologically confirmed solid tumor.
3) Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

Exclusion Criteria

1) Patients with gastric cancer or stomach excised

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pharmacokinetics
Secondary Outcome Measures
NameTimeMethod
Safety, Efficacy<br>CTCAE (ver.4.0), RECIST (ver.1.1)
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