TrialSignal
Clinical trial intelligence report
Sequential Gilteritinib in Combination With Venetoclax and Azacitidine for Patients With Newly Diagnosed Acute Myeloid Leukemia (AML) and FLT3 Mutations Ineligible for Intensive Treatment
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT06696183-Jul 28, 2026
NCT ID
NCT06696183
Status
RECRUITING
Phase
Phase 2
Sponsor
Technische Universität Dresden
Executive brief
Investment-Ready Snapshot
The clinical trial, sponsored by Technische Universität Dresden, investigates the combination of Gilteritinib, Venetoclax, and Azacitidine in patients with newly diagnosed AML harboring FLT3 mutations who are ineligible for intensive chemotherapy. This patient population represents a significant unmet medical need, as current treatment options are limited for those unable to tolerate standard induction chemotherapy. The trial's focus on optimizing dosing regimens may enhance therapeutic outcomes and improve market positioning for Gilteritinib in the competitive landscape of AML therapies. Given the increasing prevalence of AML and the growing market for targeted therapies, successful trial outcomes could lead to expanded indications and increased market share for the involved compounds.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT06696183
Indication
AML - Acute Myeloid Leukemia
Modality
small molecule
Target
FLT3 mutations in Acute Myeloid Leukemia (AML)
Intervention
Gilteritinib (GILT), Venetoclax (VEN), Azacitidine (AZA)
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.