Pegylated Interferon Alfa-2b and Nilotinib for Augmentation of Complete Molecular Response in Chronic Myeloid Leukaemia

PHASE2CompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

April 11, 2014

Primary Completion Date

January 7, 2022

Study Completion Date

January 7, 2022

Conditions
Chronic Myeloid Leukaemia
Interventions
DRUG

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.

Trial Locations (1)

5000

Royal Adelaide Hospital, Adelaide

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Merck Sharp & Dohme LLC

INDUSTRY

collaborator

Novartis Pharmaceuticals

INDUSTRY

lead

Australasian Leukaemia and Lymphoma Group

OTHER