11
Participants
Start Date
August 3, 2011
Primary Completion Date
March 14, 2013
Study Completion Date
March 14, 2013
CEP-18770
CEP-18770 will be administered per dose and schedule specified in the arm description.
Lenalidomide
Lenalidomide will be administered per dose and schedule specified in the arm description.
Dexamethasone
Dexamethasone will be administered per dose and schedule specified in the arm description.
Teva Investigational Site 201, Auckland
Teva Investigational Site 206, Hamilton
Teva Investigational Site 205, Newtown
Teva Investigational Site 200, Christchurch
Teva Investigational Site 1, Augusta
Teva Investigational Site 3, Lexington
Teva Investigational Site 2, Houston
Teva Investigational Site 204, Auckland
Teva Branded Pharmaceutical Products R&D, Inc.
INDUSTRY