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Study details
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UPDATE AML: UPdated Disease Monitoring And Treatment for Enhanced Outcomes for Pediatric AML

Joanna Yi
NCT IDNCT07059975ClinicalTrials.gov data as of Apr 2026
Phase

EARLY_PHASE1

Target enrollment

36

Study length

about 5.9 years

Ages

0.0833333333333333–30

Locations

1 site in TX

About this study

This trial is testing a treatment to see if it's safe and effective in replacing some chemotherapy cycles with other treatments for children newly diagnosed with acute myeloid leukemia (AML). The goal is to improve survival while reducing long-term side effects. Researchers will monitor participants for up to three years after enrollment.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Receive Intrathecal triple
  • 2.SOC
  • 3.Take Asparaginase Erwinia Chrysanthemi (recombinant)
  • +3 more
PhaseEARLY_Phase 1
DrugAsparaginase Erwinia Chrysanthemi (recombinant)
Routeinjection
Primary goalTolerability rate of Ida-FLA

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low13%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS, cytarabine, etoposide, fludarabine, Antineoplastic Agent [TC] (Topoisomerase 2 Inhibitors), venetoclax

Drug routes

injection (Injection), injection, intravenous, oral (Oral Capsule), oral

Endpoints

Primary: Tolerability rate of Ida-FLA, Tolerability rate of VIA for HR patients, Tolerability rate of VIA for IR patients

Secondary: 3 year event-free survival, 3 year overall survival, Complete remission rate, Tolerability rate of intensified regimen as a whole for HR patients, Tolerability rate of intensified regimen as a whole for IR patients

Body systems

Oncology