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Clinical Trials in Germany / NCT06696183
Recruiting Phase 2

Gilteritinib in Combination With Venetoclax and Azacitidine for AML Patients With FLT3 Mutations Ineligible for Intensive Treatment

NCT06696183 · tracked via the Priya Life Science Germany tracker
Phase
Phase 2
Started
2025-04-25
Last updated
2025-05-29

Condition(s) studied

AML - Acute Myeloid Leukemia

Investigational drug(s) / intervention(s)

Gilteritinib (GILT) →Venetoclax (VEN) →Azacitidine (AZA) →

Gilteritinib (GILT): 80 mg

Venetoclax (VEN): 400 mg

Azacitidine (AZA): 75 mg/m²

Study summary

Explore the best tolerable and efficacious dose of Gilteritinib when combined with standard treatment with Venetoclax and Azacitidine in AML patients with FLT3 mutations which are ineligible for intensive chemotherapy

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Main Inclusion Criteria: * Newly diagnosed AML (according to WHO 2022 or ICC 2022 criteria) with a minimum BM blast count of \>=20%, excluding APL * FLT3 mutation at initial diagnosis * Ineligibility of standard induction chemotherapy * Pre-treatment with approved combination of Venetoclax + Azacitidine (one cycle only) Main Exclusion Criteria: * R/R AML * Previous treatment for AML (except HU and/or one cycle VEN+AZA according to SOC) * Previous treatment with Gilteritinib * Known active CNS involvement * QTcF \>450 ms or long QT Syndrome at screening * Treatment with concomitant strong CYP3A inducers or St. John's wort

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Technische Universität Dresden Dresden Germany Recruiting

More Technische Universität Dresden trials in Germany

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06696183 on ClinicalTrials.gov ↗ ← All trials in Germany