A Phase II Open-Label, Single Center Trial of Oral Decitabine-Cedazuridine (DEC-C) (Inqovi®) in Combination With Thioguanine (Tabloid®) in Patients With Relapsed or Refractory (R/R) Acute Myeloid Leukemia (AML)
The trial, sponsored by Columbia University, aims to evaluate the safety and efficacy of a combination therapy involving oral decitabine-cedazuridine and thioguanine in patients with relapsed or refractory AML. The market for AML therapies is significant, with a high unmet need for effective treatments, particularly in relapsed cases where current options yield low response rates. The withdrawal of the trial due to difficulties in enrollment may indicate challenges in patient recruitment, potentially impacting the commercial viability of this combination therapy. Competitively, the landscape includes established therapies and emerging agents, necessitating a robust differentiation strategy for any successful outcomes from this trial.
Indication: Acute Myeloid Leukemia
Modality: small molecule
Target: Oral decitabine-cedazuridine (Inqovi®) and thioguanine (Tabloid®) target the epigenetic regulation of gene expression and DNA synthesis in acute myeloid leukemia (AML) cells.
Sponsor: Columbia University
Source URL: ClinicalTrials.gov
Source updated: Detailed source ingestion pending
Ingested: Jul 21, 2026
Model: trialsignal-ai-v1
Validation: validated
Matched by target_normalized: Oral decitabine-cedazuridine (Inqovi®) and thioguanine (Tabloid®) target the epigenetic regulation of gene expression and DNA synthesis in acute myeloid leukemia (AML) cells.
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Condition raw: Acute Myeloid Leukemia
Condition normalized: Acute Myeloid Leukemia
Modality raw: small molecule
Modality normalized: small molecule
Target raw: Oral decitabine-cedazuridine (Inqovi®) and thioguanine (Tabloid®) target the epigenetic regulation of gene expression and DNA synthesis in acute myeloid leukemia (AML) cells.
Target normalized: Oral decitabine-cedazuridine (Inqovi®) and thioguanine (Tabloid®) target the epigenetic regulation of gene expression and DNA synthesis in acute myeloid leukemia (AML) cells.