head and neck cancer
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients treated with intravenous cetuximab for head and neck cancer 2. Patients receiving written informed consent
Exclusion criteria
Exclusion criteria: 1. Patients discontinuing intravenous cetuximab 2. Patients who are judged by physicians as inappropriate for study enrollment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Serum concentration of cetuximab before dosing on week 4 or later | — |
Countries
Japan
Contacts
Hamamatsu University School of Medicine Department of Hospital pharmacy