TrialSignal
Clinical trial intelligence report
A Phase 2, Prospective, Multi-center Intervention Trial in Patients With Acute Myeloid Leukemia Secondary to Myeloproliferative Neoplasms Unfit for Intensive Chemotherapy Investigating a Treatment Combination Including Decitabine and Venetoclax
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT04763928-Jul 28, 2026
NCT ID
NCT04763928
Status
ACTIVE_NOT_RECRUITING
Phase
Phase 2
Sponsor
Gruppo Italiano Malattie EMatologiche dell'Adulto
Executive brief
Investment-Ready Snapshot
The trial investigates a combination therapy of Venetoclax (VEN) and Decitabine (DEC) for patients with acute myeloid leukemia (AML) secondary to myeloproliferative neoplasms (MPNs) who are unfit for intensive chemotherapy. Given the high unmet need in this patient population, successful outcomes could position this combination regimen as a significant treatment option in a niche market. The competitive landscape includes existing therapies for AML, but the specific targeting of sAML with this combination may provide a unique selling proposition. Diligence should focus on the trial's efficacy and safety data, as well as potential regulatory pathways for accelerated approval based on the high unmet need.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04763928
Indication
Acute Myeloid Leukemia
Modality
small molecule
Target
BCL-2 and DNA methyltransferase
Intervention
Venetoclax+Decitabine
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.