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Analysis on individual difference in pharmacokinetics of aprepitant and its metabolites, and investigation on predictive parameters of aprepitant response and adverse effects in Japanese patiens

Not Applicable
Recruiting
Conditions
head and neck cancer
Registration Number
JPRN-UMIN000041069
Lead Sponsor
Department of Hospital pharmacy Amaterasu University School of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
150
Inclusion Criteria

Not provided

Exclusion Criteria

1. Patients discontinuing aprepitant 2. Patients who are judged by physicians as inappropriate for study enrollment

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Plasma concentrations of aprepitant and its metabolites at 24 hours after the last oral administration of aprepitant.
Secondary Outcome Measures
NameTimeMethod
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