13
Participants
Start Date
July 31, 2008
Primary Completion Date
September 30, 2010
Study Completion Date
September 30, 2010
Erlotinib
Erlotinib 150mg daily, continuously, until disease progression or the appearance of unacceptable toxicity
Bevacizumab
Bevacizumab (IV) 15 mgr/Kgr on day 1 every 3 weeks until disease progression or the appearance of unacceptable toxicity
University Hospital of Heraklion, Heraklion
University General Hospital of Alexandroupolis, Dep of Medical Oncology, Alexandroupoli
"Laikon General Hospital, Medical Oncology Unit, Propedeutic Dep of Internal Medicine", Athens
401 Military Hospital, Medical Oncology Unit, Athens
Air Forces Military Hospital, Dep of Medical Oncology, Athens
"IASO General Hospital of Athens, 1st Dep of Medical Oncology", Athens
Sismanogleio General Hospital, 1st, 2nd Dep of Pulmonary Diseases, Athens
"Sotiria General Hospital, 1st, 3rd, 8th Dep of Pulmonary Diseases", Athens
"Metaxa's Anticancer Hospital of Piraeus,1st Dep of Medical Oncology", Piraeus
"Theagenion Anticancer Hospital of Thessaloniki", Thessaloniki
Lead Sponsor
University Hospital of Crete
OTHER
Hellenic Oncology Research Group
OTHER