A Study to Assess the Efficacy and Safety of Lenalidomide in Combination With Cetuximab in Pre-treated Patients With KRAS Mutant Colorectal Cancer

PHASE2TerminatedINTERVENTIONAL
Enrollment

51

Participants

Timeline

Start Date

December 31, 2009

Primary Completion Date

January 31, 2011

Study Completion Date

January 31, 2011

Conditions
Colorectal Cancer
Interventions
DRUG

cetuximab

Intravenous infusions of cetuximab (400 mg/m\^2 Cycle 1 Day 1, thereafter 250 mg/m\^2), administered on days 1, 8, 15 and 22 of each 28 day cycle.

DRUG

lenalidomide

Daily oral lenalidomide 25mg on days 1 to 28 of each 28 day cycle

Trial Locations (17)

Unknown

Flinders Medical Centre, Dept. of Oncology, Bedford Park

UZ Antwerpen Dept. of Medical Oncology, Antwerp

ULB Erasme Service de Gastroenterologie, Brussels

Grand hôpital de Charleroi, Oncologie, Charleroi

Algemeen Ziekenhuis Maria Middelares, Ghent

Universitaire Ziekenhuis Gasthuisberg K.U. Leuven Gastroenterologie, Oncologie, Leuven

Centre Hospitalier Universitaire Sart Tilman Liège, Liège

Klinikum Oldenburg gGmbH Klinik für Innere Medizin II, Oldenburg

Azienda Osperdaliero Universitaria Riuniti Umberto I-GM Lancisi-G. Salesi di Ancona Clinica di Oncologia Medica, Ancona

Azienda Ospedaliera Universitaria San Martino Unità Operativa Oncologia Medica, Genova

Azienda Ospedaliera Niguarda Ca' Grande, Oncologia Medica Falck, Milan

Hospital Vall D'Hebron Servicio de Oncología. Unidad de ensayos clínicos, Barcelona

Hospital Universitario Marques de Valdecilla Servicio de Oncología, Santander

Hospital Clinico Universitario de Valencia Servicio de Oncologia, Valencia

Östra Sjukhuset Kirurgkliniken, Gothenburg

Karolinska University Hospital, Solna, Karolinska Institutet Dept of Oncology, Stockholm

Akademiska Sjukhuset Onkologkliniken, Uppsala

Sponsors
All Listed Sponsors
lead

Celgene Corporation

INDUSTRY