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Clinical trial intelligence report
Clinical Study Protocol of Venetoclax Combined With Azacitidine and Harringtonine in the Treatment of Secondary Acute Myeloid Leukemia
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT05513131-Jul 28, 2026
NCT ID
NCT05513131
Status
UNKNOWN
Phase
Phase 2
Sponsor
The First Affiliated Hospital with Nanjing Medical University
Executive brief
Investment-Ready Snapshot
The clinical trial evaluates a novel combination therapy of Venetoclax, Azacitidine, and Harringtonine for secondary acute myeloid leukemia (sAML), a patient population with limited treatment options. Given the FDA's prior approval of Venetoclax in combination with Azacitidine for elderly patients with newly diagnosed AML, this trial could position the combination as a competitive treatment option for younger patients with sAML. The anticipated enrollment of 30 patients and the focus on efficacy and safety could provide valuable data to support potential market entry. The trial's outcomes may influence treatment guidelines and establish a new standard of care, thereby impacting market dynamics and competitive positioning in the hematologic oncology space.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05513131
Indication
Secondary Acute Myeloid Leukemia
Modality
small molecule
Target
BCL-2 (B-cell lymphoma 2) inhibition, with additional effects from Azacitidine and Harringtonine on tumor cell apoptosis and protein synthesis inhibition.
Intervention
Venetoclax;Azacitidine;Homoharringtonine
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.