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Clinical Trial Summary

Retrospective, non-interventional observational cohort study conducted among patients with CML.


Clinical Trial Description

A retrospective, non-interventional cohort study was used to address the study objectives. A cohort of adult patients with CML who were treated with TKIs were identified using the IBM® MarketScan® Commercial and Medicare Supplemental databases (commercial claims; the MarketScan database) to have a better understanding of real-world treatment patterns, HRU and healthcare costs among patients with CML treated with later lines of therapy (i.e., third line or later). For Phase I, the IBM® MarketScan® Commercial Claims and Encounters and Medicare Supplemental Databases were used (commercial claims). The commercial claims covered the period from 01/01/2001 to 06/30/2019. The study consisted of the following periods: - The baseline period was defined as the 6-month period before the first line therapy initiation for CML. - The observation period was defined as the period of at least 12 months from the first CML diagnosis to the end of data availability or end of health plan coverage, whichever occurs first; the observation period varied by patient. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05476562
Study type Observational
Source Novartis
Contact
Status Completed
Phase
Start date March 8, 2021
Completion date October 15, 2021

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