Cellular phase chronic idiopathic myelofibrosis

disease
On this page

Also known as chronic idiopathic myelofibrosis, cellular phasechronic idiopathic myelofibrosis, Prefibrotic stagePMFPESPrefibrotic/Early Primary myelofibrosisprimary myelofibrosis, Prefibrotic stageprimary myelofibrosis, Prefibrotic/early stage

Summary

Cellular phase chronic idiopathic myelofibrosis (MONDO:0004463) is a disease and 10 clinical trials. Top therapeutic interventions include aspirin, ropeginterferon alfa-2b, and ruxolitinib. A subtype of primary myelofibrosis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 10

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namecellular phase chronic idiopathic myelofibrosis
Mondo IDMONDO:0004463
DOIDDOID:8106
NCITC41237
UMLSC1516553
MedGen275741
GARD0024019
Is cancer (heuristic)no

Also known as: chronic idiopathic myelofibrosis, cellular phase · chronic idiopathic myelofibrosis, Prefibrotic stage · PMFPES · Prefibrotic/Early Primary myelofibrosis · primary myelofibrosis, Prefibrotic stage · primary myelofibrosis, Prefibrotic/early stage

Disease family

This is a subtype of primary myelofibrosis. 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 body system or component › hematologic disorderanemiaaplastic anemiaacquired aplastic anemiaprimary myelofibrosiscellular phase chronic idiopathic myelofibrosis

Related subtypes (3): familial myelofibrosis, panostotic fibrous dysplasia, myelofibrosis with myeloid metaplasia

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: 10.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified6
PHASE31
PHASE1/PHASE21
PHASE21
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05198960PHASE3RECRUITINGAVAJAK: Apixaban/Rivaroxaban Versus Aspirin for Primary Prevention of Thrombo-embolic Complications in JAK2V617F-positive Myeloproliferative Neoplasms
NCT03862157PHASE1/PHASE2ACTIVE_NOT_RECRUITINGAzacitidine, Venetoclax, and Pevonedistat in Treating Patients With Newly Diagnosed Acute Myeloid Leukemia
NCT04988815PHASE2UNKNOWNRopeginterferon Alfa 2b for Early Myelofibrosis
NCT02528877PHASE1WITHDRAWNRuxolitinib Phosphate, Tacrolimus and Sirolimus in Preventing Acute Graft-versus-Host Disease During Reduced Intensity Donor Hematopoietic Cell Transplant in Patients With Myelofibrosis
NCT04942080Not specifiedRECRUITINGInterest of CALR Allele Burden in Diagnosis and Follow-up of Patients With CALR Mutated Myeloproliferative Syndromes (CALRSUIVI)
NCT05882773Not specifiedRECRUITINGAsian Myeloproliferative Neoplasm (MPN) Registry
NCT03116542Not specifiedUNKNOWN18F-FLT (PET/CT) in Prefibrotic/Early Primary Myelofibrosis and Essential Thrombocythemia
NCT03121599Not specifiedTERMINATED18F-FLT (PET/CT) in Pediatrics With Myeloproliferative Neoplasms
NCT03869476Not specifiedCOMPLETEDPilot Study for the Development of a Diagnostic Score to Differentiate Myeloproliferative Neoplasms.
NCT06371573Not specifiedCOMPLETEDUltrasound Examination for Spleen Volume Evaluation in Myeloproliferative Neoplasms

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
ASPIRIN41
ROPEGINTERFERON ALFA-2B41
RUXOLITINIB41
PEVONEDISTAT31