A multicenter, open label study of Nilotinib in CML patients PH + with imatininb resistant in blast crisis, accelerated phase or chronic phase. The main purpose is evaluate the safety and efficacy of Nilotinib.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
6
Hospital San José, Bogotá, Colombia
Bogotá, Colombia
Banco Municipal de Sangre
Caracas, Venezuela
Maintain and monitor long-term hematological and cytogenetic responses previously obtained by patients participating in the CAMN107A2109 study.
Time frame: between 6 and 12 months
To evaluate the rate of any durable cytogenetic response and Complete cytogenetic response
Time frame: 24 months
To evaluate the rate of molecular response every 3 months, until 24th month of treatment or end of study
Time frame: 24 months
To follow loss of HR (after previous confirmed HR for AP and CHR for CP)
Time frame: 3, 6 and 12 months
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