A Study Of Treatment Patterns And Clinical Outcomes In Patients Diagnosed With Acute Myeloid Leukemia Who Received Mylotarg in the Real-World
Completed
Conditions studied: Leukemia, Myeloid, Acute
In brief
The aim of this observational study is to describe treatment patterns and effectiveness outcomes in a sample of oncology patients treated for AML with Mylotarg through up to two additional relapsed/refractory (R/R)-based lines of therapy (through third-line therapy). The study will use United States oncology electronic medical record (EMR) data. All study data are secondary data and will have been collected retrospectively from existing clinical data originally collected as part of routine care.
Key facts
- Study ID
- NCT04337138
- Run by
- Pfizer
- People needed
- 32
- Starts
- 2020-04-07
- Expected to finish
- 2020-07-31
- Last updated by the study team
- 2021-08-09
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Confirmed diagnosis of acute myeloid leukemia (AML) on or after 01 December 2014 through Clinical Research Nurse (CRN) review of provider documentation of AML diagnosis in the medical record;
- Receipt of Mylotarg at any point during first three lines of therapy following initial AML diagnosis;
- Age greater than or equal to 18 years at initial diagnosis of AML.
You may not qualify if…
- Record of 1 or more of the following confounding diagnoses at any point before or after AML diagnosis: Acute lymphoblastic leukemia; acute promyelocytic leukemia, aggressive systemic mastocytosis; hypereosinophilic syndrome and/or chronic eosinophilic leukemia; dermatofibrosarcoma protuberans; gastrointestinal stromal tumors.
Where it is running
- Pfizer Investigational Site — New York, New York, United States
Full record on ClinicalTrials.gov
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