A Rollover Protocol of Dacomitinib For Patients In Japan

PHASE2CompletedINTERVENTIONAL
Enrollment

7

Participants

Timeline

Start Date

July 10, 2015

Primary Completion Date

May 30, 2019

Study Completion Date

May 30, 2019

Conditions
NSCLC
Interventions
DRUG

Dacomitinib

Starting at the current dose level in the prior study. Dose reductions and re-escalations are allowed based on tolerability. Patients may continue to be treated with dacomitinib on this protocol as long as there is evidence of clinical benefit in the judgment of the investigator.

Trial Locations (6)

9208641

Kanazawa University Hospital, Kanazawa

710-8602

Kurashiki Central Hospital, Kurashiki

534-0021

Osaka City General Hospital Department of Clinical Oncology, Osaka

589-8511

Kindai University Hospital, Sayama

411-8777

Shizuoka Cancer Center, Suntougun

135-8550

Cancer Institute Hospital,Japanese Foundation for Cancer Research, Koto-Ku

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT02382796 - A Rollover Protocol of Dacomitinib For Patients In Japan | Biotech Hunter | Biotech Hunter