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Phase II Trial of Arsenic Trioxide With Ascorbic Acid in the Treatment of Adult Non-APL Acute Myelogenous Leukemia
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 19, 2026
NCT ID
NCT00184054
Status
TERMINATED
Phase
Phase 2
Sponsor
University of Southern California
Executive brief
Investment-Ready Snapshot
The combination of arsenic trioxide and ascorbic acid presents a novel therapeutic approach for treating refractory non-APL acute myelogenous leukemia (AML). Given the limited treatment options for this patient population, successful outcomes could position this combination as a competitive alternative in the AML market. However, the trial was terminated due to competing studies, which may indicate a saturated or rapidly evolving landscape for AML therapies. Further diligence is required to assess ongoing studies and potential market entry strategies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT00184054
Indication
Acute Myelogenous Leukemia
Modality
small molecule
Target
Arsenic trioxide targets multiple pathways involved in apoptosis and differentiation in cancer cells, particularly through the induction of reactive oxygen species (ROS) and modulation of various signaling pathways.
Intervention
Arsenic Trioxide (ATO), Ascorbic Acid
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.