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NCT00184054TERMINATEDanonymous

Phase II Trial of Arsenic Trioxide With Ascorbic Acid in the Treatment of Adult Non-APL Acute Myelogenous Leukemia

Sponsor

Source record

University of Southern California

Phase

Source record

Phase 2

Modality

AI-normalized

small molecule

Target

AI-normalized

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.

Indication / condition

AI-normalized

Acute Myelogenous Leukemia

Intervention

Source record

Arsenic Trioxide (ATO), Ascorbic Acid

Source & freshness

Source record

NCT ID

NCT00184054

Original source

ClinicalTrials.gov

Source last updated

Jul 25, 2014

Ingested at

Jun 19, 2026

Internal sync

Jun 19, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT00184054

Title

Phase II Trial of Arsenic Trioxide With Ascorbic Acid in the Treatment of Adult Non-APL Acute Myelogenous Leukemia

Sponsor

University of Southern California

Status

TERMINATED

Phase

Phase 2

Condition raw

Acute Myelogenous Leukemia

Condition normalized

Acute Myelogenous Leukemia

Modality raw

small molecule

Modality normalized

small molecule

Target raw

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.

Target normalized

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.

Interventions

Arsenic Trioxide (ATO), Ascorbic Acid

Public preview

Source record

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.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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