Japanese CML treatment patterns revealed in large database study
NCT ID NCT07150793
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study looked at how 754 people with chronic myeloid leukemia (CML) in Japan were treated with drugs called tyrosine kinase inhibitors (TKIs) between 2011 and 2019. Researchers used a hospital database to track which TKIs patients received, how often they switched or stopped treatment, and the costs involved. The goal was to describe real-world treatment patterns, not to test a new therapy.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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754 people
The number who actually took part.
- Started
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Jul 2022
- Finished
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Feb 2023
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
This was a retrospective, non-interventional cohort study.
- Ages
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15 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Patients who met all the below inclusion criteria and none of the exclusion criteria were included in the study. Inclusion criteria: * Patients who had at least one TKI prescription during the selection period, * a confirmed diagnosis of chronic phase CML recorded before or at the index date, * were aged 15 years or older at the index date, and * had at least 12-months continuous pre-index period. Exclusion criteria: * Patients who had at least one TKI prescription in the 12 months preceding the index date (washout period to catch the 1st line of treatment \[LoT\]), * a confirmed diagnosis of CML blast crisis or accelerated phase recorded prior to, at, or within 6 months after the index date, * a confirmed diagnosis of acute myeloid leukemia (AML) or acute lymphoblastic leukemia (ALL) within 6 months after the index date, * a medical record of chemotherapy (not including hydroxyurea) within 6 months after the index date, * a stem cell transplant procedure recorded during the pre-index period.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Novartis
East Hanover, New Jersey, 07936, United States