| Protocol No. | UW25098 |
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|---|---|---|---|
| Principal Investigator | Lee-Miller, Cathy | ||
| Phase | N/A | ||
| Age Group | Both | ||
| Management Group(s) | Pediatric Oncology | ||
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Title
Description
Objective
Treatment 10 adolescent patients (ages 10-19) will be purposively sampled from American Family Children’s Hospital in Madison, Wisconsin.
Key Eligibility
Eligible participants must (a) be a patient between the ages of 10 to 19 with a diagnosis of acute lymphoblastic leukemia who is either currently receiving blinatumomab or received blinatumomab within the past one year, (b) received at least two weeks of the infusion, (c) be able to provide parental consent if less than age 18 as well as assent if less than age 18, and (d) be English speaking. The ages of 10 to 19 were selected due to ages 10 and above being considered developmentally appropriate to answer questions for the interview. We also routinely see patients up to age 19 at our center.
Applicable Disease Sites
Participating Institutions
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