51
Participants
Start Date
September 30, 2009
Primary Completion Date
August 31, 2017
Study Completion Date
August 31, 2017
lenalidomide, bendamustine, rituximab
"Phase I: Maximally tolerable dose of lenalidomide will be determined, starting with 5 mg per day, and up to maximally 25 mg per day. This treatment is given in combination with bendamustine and rituximab.~Phase II: Determination of progression free survival with treatment with lenalidomide (dosing determined in phase I) in combination with bendamustine and rituximab."
lenalidomide, bendamustine, rituximab
lenalidomide: day 1-21, maximum 13 cycles bendamustine: days 1-2, cycle 1-6 rituximab: day1, cycle 1-6
Århus University Hospital, Aarhus
Herlev Hospital, Copenhagen
Rigshospitalet, Department of Hematology, Copenhagen
Helsinki University Central Hospital, Helsinki
Haukeland University Hospital, Department of Oncology, Bergen
Norwegian Radium Hospital, Oslo
Ulleval University Hospital, Department of Oncology, Oslo
University Hospital of Stavanger, Department of Haematology and Oncology, Stavanger
University Hospital of Tromso, Department of Oncology, Tromsø
Sahlgrenska University Hospital, Department of Hematology, Gothenburg
University Hospital Linköping, Department of Hematology, Linköping
Sunderbyn Hospital, Department of Medicine, Luleå
University Hospital Lund, Department of Oncology, Lund
Karolinska University Hospital, Department of Hematology, Stockholm
Sundsvall Hospital, Department of Medicine, Sundsvall
University Hospital of Norrland, Department of Oncology, Umeå
Uppsala University Hospital, Department of Oncology, Uppsala
Collaborators (2)
Mundipharma Pte Ltd.
INDUSTRY
Celgene
INDUSTRY
Roche Pharma AG
INDUSTRY
Lund University Hospital
OTHER