60
Participants
Start Date
April 11, 2014
Primary Completion Date
January 7, 2022
Study Completion Date
January 7, 2022
Nilotinib, Pegylated interferon alpha-2b, Imatinib
All patients joining the study will receive treatment with oral nilotinib at 300mg twice daily. This will be given as monotherapy for 3 months initially, prior to commencement of combination therapy with Pegylated interferon alpha-2b added to nilotinib. Patients intolerant of nilotinib will have the option of switching to imatinib.
Royal Adelaide Hospital, Adelaide
Collaborators (1)
Merck Sharp & Dohme LLC
INDUSTRY
Novartis Pharmaceuticals
INDUSTRY
Australasian Leukaemia and Lymphoma Group
OTHER