Monocytic leukemia

disease
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Summary

Monocytic leukemia (MONDO:0004600) is a cancer and 6 clinical trials. Top therapeutic interventions include ascorbic acid and hyaluronidase (human recombinant). A subtype of leukemia — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Classification: Cancer
  • Clinical trials: 6

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namemonocytic leukemia
Mondo IDMONDO:0004600
DOIDDOID:8527
ICD-10-CMC93
SNOMED CT188744006
UMLSC0598894
MedGen109338
GARD0024074
Is cancer (heuristic)yes

Disease family

This is a subtype of leukemia. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumorneoplastic disease or syndromeneoplasmhematopoietic and lymphoid system neoplasmhematopoietic and lymphoid cell neoplasmleukemiamonocytic leukemia

Related subtypes (11): chronic leukemia, chronic erythremia, testicular leukemia, central nervous system leukemia, aleukemic leukemia, splenic manifestation of leukemia, childhood leukemia, myeloid leukemia, lymphoid leukemia, acute leukemia, mast cell leukemia

Subtypes (2): chronic monocytic leukemia, acute monocytic leukemia

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 6.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE22
PHASE12
PHASE1/PHASE21
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07292272PHASE2RECRUITINGHalt Aging in Survivors of Blood Cancers
NCT03613727PHASE2COMPLETEDTherapeutic Use of Intravenous Vitamin C in Allogeneic Stem Cell Transplant Recipients
NCT05282459PHASE1/PHASE2COMPLETEDEnasidenib in MDS &Non-proliferative Chronic Myelomonocytic Leukemia w/o IDH2 Mutation
NCT06429449PHASE1RECRUITINGMitoxantrone for Venetoclax Resistant Acute Myeloid Leukemia
NCT04714372PHASE1COMPLETEDFT538 in Combination With Daratumumab in AML Acute Myeloid Leukemia
NCT05871008Not specifiedACTIVE_NOT_RECRUITINGIntegrated Actionable Aging Assessment for Cancer Patients Pilot

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
ASCORBIC ACID41
HYALURONIDASE (HUMAN RECOMBINANT)41