Improving the efficacy and safety in the treatment of resistant forms of chronic myelogenous leukemia, including the variant with T315I mutation
Mutation T315I under sight
Efficacy against clones of CML tumor cells with T315I mutation in the proto-oncogene BCR-ABL
Suppression of the emergence of resistance
Suppression of the emergence of resistant forms of CML in experiments with directed mutagenesis of CML tumor cells
When resistant to two or more Abl inhibitors
Investigating efficacy and safety in patients resistant to at least two Abl inhibitors
Advanced phases of CML
Investigating the efficacy in the accelerated phase and blast crisis and potentials in the therapy of Ph + acute lymphoblastic leukemia
For Patients
When deciding to participate in the trial, please, contact the study coordinators of one of the two clinical sites directly to see if you are eligible for the trial: A multicenter, open label cohort Phase 1 dose escalation study to evaluate safety, tolerability, pharmacokinetics and preliminary efficacy of PF-114 mesylate for oral administration in adult patients with Philadelphia chromosome positive (Ph+) chronic myeloid leukemia (CML), which is resistant to the 2-nd generation Bcr-Abl inhibitors or has T315I mutation in the BCR-ABL gene. The information on the Study is listed on registry and results database of publicly and privately supported clinical studies of human participants conducted around the world — the ClinicalTrials.gov
Please, see the Informed Consent Form to participate in the Clinical Trial.