A Post Marketing Surveillance Study of Cetuximab in Patients With Squamous Cell Carcinoma of Head and Neck (SCCHN)

CompletedOBSERVATIONAL
Enrollment

215

Participants

Timeline

Start Date

September 30, 2010

Primary Completion Date

December 31, 2013

Study Completion Date

December 31, 2013

Conditions
Carcinoma, Squamous Cell of Head and Neck
Interventions
OTHER

No Intervention

Subjects administered with Cetuximab, once weekly by intravenous infusion at a first dose of 400 milligram per square meter (mg/m\^2) body surface area for 120 minutes infusion period and subsequently at a dose of 250 mg/m\^2 for 60 minutes infusion period, will be observed. The maximum infusion rate must not exceed 10 milligram per minute (mg/min).

Trial Locations (1)

Unknown

Liouying Chi-Mei Hospital, Liuying

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Choice Pharma Taiwan

UNKNOWN

lead

Merck KGaA, Darmstadt, Germany

INDUSTRY