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Disease · MONDO_0009692

primary myelofibrosis

6 sourcesdiseases-2026-09-18-0.1.0

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ConductScience Library. primary myelofibrosis. Diseases, record MONDO_0009692. Release diseases-2026-09-18-0.1.0, 18 Sept 2026. https://conductscience.org/library/diseases/MONDO_0009692

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Disease

Names and IDs as Open Targets gives them. Its IDs in MeSH, Orphanet, the Disease Ontology and the NCI Thesaurus are those Open Targets states for it.

Name
primary myelofibrosis
Open Targets
Open Targets ID
MONDO_0009692
Open Targets
Other names
AMM, Agnogenic myeloid metaplasia, CIMF, aleukemic myelosis, bone marrow fibrosis, chronic idiopathic myelofibrosis, idiopathic bone marrow fibrosis, idiopathic myelofibrosis, megakaryocytic myelosclerosis, myelofibrosis with myeloid metaplasia, myelofibrosis with myeloid metaplasia, somatic, myelofibrosis, somatic, myelosclerosis, myelosclerosis with myeloid metaplasia, osteomyelofibrosis
Open Targets
Disease Ontology
DOID:4971
Disease Ontology
MeSH
D055728
MeSH
NCI Thesaurus
C2862
NCI Thesaurus
Orphanet
ORPHA:824
Orphanet
Highest stage of its drugs
Approval, for 5 of its 63 drugs, from DailyMed, EMA Human Drugs and FDA
Open Targets

Drugs63

The drugs Open Targets' clinical reports study for the disease, the highest stage first, then the most trial reports. The stage is Open Targets', the highest any of its sources reports for the pair, and each row names the sources that report it.

DrugChEMBL IDTypeOpen Targets' stageStage reported byReportsOf them trialsTrials shown hereSource
FEDRATINIBCHEMBL1287853Small moleculeApprovalEMA Human Drugs877Drugs and targets
FEDRATINIB HYDROCHLORIDECHEMBL4297216Small moleculeApprovalFDA100Drugs and targets
MOMELOTINIB DIHYDROCHLORIDECHEMBL2219411Small moleculeApprovalFDA100Drugs and targets
PACRITINIB CITRATECHEMBL5095049Small moleculeApprovalFDA100Drugs and targets
RUXOLITINIB PHOSPHATECHEMBL1795071Small moleculeApprovalDailyMed100Drugs and targets
RUXOLITINIBCHEMBL1789941Small moleculePhase 3ClinicalTrials.gov151515Drugs and targets
MOMELOTINIBCHEMBL1078178Small moleculePhase 3ClinicalTrials.gov888Drugs and targets
PACRITINIBCHEMBL2035187Small moleculePhase 3ClinicalTrials.gov555Drugs and targets
ROPEGINTERFERON ALFA-2BCHEMBL4297819ProteinPhase 3ClinicalTrials.gov332Drugs and targets
PEGINTERFERON ALFA-2ACHEMBL1201560ProteinPhase 3ClinicalTrials.gov221Drugs and targets

1 to 10 of 63

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Targets87

The targets ChEMBL's mechanism records give for the disease's drugs, through Open Targets, the most drugs first. A mechanism record says what a drug acts on, not that the target causes the disease.

TargetProteinIts drugs that act on itMechanismsHighest stage of those drugsGene in GenesSource
JAK2Tyrosine-protein kinase JAK210Tyrosine-protein kinase JAK2 inhibitorApprovalhttps://conductscience.org/library/genes/3717Drugs and targets
FLT3Receptor-type tyrosine-protein kinase FLT35Tyrosine-protein kinase receptor FLT3 inhibitorApprovalhttps://conductscience.org/library/genes/2322Drugs and targets
IFNAR1Interferon alpha/beta receptor5Interferon alpha/beta receptor agonist; Interferon alpha/beta receptor positive modulatorPhase 3https://conductscience.org/library/genes/3454Drugs and targets
IFNAR2Interferon alpha/beta receptor5Interferon alpha/beta receptor agonist; Interferon alpha/beta receptor positive modulatorPhase 3https://conductscience.org/library/genes/3455Drugs and targets
JAK1Tyrosine-protein kinase JAK14Tyrosine-protein kinase JAK1 inhibitorApprovalhttps://conductscience.org/library/genes/3716Drugs and targets
KITMast/stem cell growth factor receptor Kit4Stem cell growth factor receptor inhibitorPhase 2https://conductscience.org/library/genes/3815Drugs and targets
PDGFRBPlatelet-derived growth factor receptor4Platelet-derived growth factor receptor beta inhibitor; Platelet-derived growth factor receptor inhibitorPhase 2https://conductscience.org/library/genes/5159Drugs and targets
ABL1Bcr/Abl fusion protein3Bcr/Abl fusion protein inhibitor; Tyrosine-protein kinase ABL inhibitorPhase 2https://conductscience.org/library/genes/25Drugs and targets
ACVR1Activin receptor type-13Activin receptor type-1 inhibitorApprovalhttps://conductscience.org/library/genes/90Drugs and targets
CRBNCRL4(CRBN) E3 ubiquitin ligase3CRL4(CRBN) E3 ubiquitin ligase inhibitor; CRL4(CRBN) E3 ubiquitin ligase modulatorPhase 2https://conductscience.org/library/genes/51185Drugs and targets

1 to 10 of 87

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Trials65

Trials an Open Targets clinical report links to the disease, posted results first, then the largest. A trial is shown when the release's checks confirm its link to the disease and Drugs and targets shows its link to one of the disease's drugs.

TrialTitlePhaseParticipantsResults first postedConditionsDrugsLinked bySource
NCT01969838Momelotinib Versus Ruxolitinib in Subjects With MyelofibrosisPhase 34322023-05-12Primary Myelofibrosis, Post-Polycythemia Vera Myelofibrosis, Post-Essential Thrombocythemia MyelofibrosisMOMELOTINIB, RUXOLITINIBIts record names the diseaseClinicalTrials.gov
NCT01773187Pacritinib Versus Best Available Therapy to Treat MyelofibrosisPhase 33272020-09-29Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis, Post-essential Thrombocythemia MyelofibrosisPACRITINIBIts record names the diseaseClinicalTrials.gov
NCT02055781Pacritinib Versus Best Available Therapy to Treat Patients With Myelofibrosis and ThrombocytopeniaPhase 33112021-11-18Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis, Post-essential Thrombocythemia MyelofibrosisPACRITINIBIts record names the diseaseClinicalTrials.gov
NCT00952289COntrolled MyeloFibrosis Study With ORal JAK Inhibitor Treatment: The COMFORT-I TrialPhase 33092012-01-24MPN (Myeloproliferative Neoplasms)RUXOLITINIBIts record names the diseaseClinicalTrials.gov
NCT00934544Controlled Myelofibrosis Study With Oral Janus-associated Kinase (JAK) Inhibitor Treatment-II: The COMFORT-II TrialPhase 32192012-05-30MyelofibrosisRUXOLITINIBIts record names the diseaseClinicalTrials.gov
NCT03952039
An Efficacy and Safety Study of Fedratinib Compared to Best Available Therapy in Subjects With DIPSS-intermediate or High-risk Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis, or Post-essential Thrombocythemia Myelofibrosis and Previously Treated With Ruxolitinib
Phase 32022024-01-30Primary Myelofibrosis, Post-Polycythemia Vera, MyelofibrosisFEDRATINIBIts record names the diseaseClinicalTrials.gov
NCT04173494A Study of Momelotinib Versus Danazol in Symptomatic and Anemic Myelofibrosis Participants (MOMENTUM)Phase 31952022-12-22Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis, Post-essential Thrombocythemia MyelofibrosisDANAZOL, MOMELOTINIBIts record names the diseaseClinicalTrials.gov
NCT02101268Efficacy of Momelotinib Versus Best Available Therapy in Anemic or Thrombocytopenic Subjects With Primary Myelofibrosis (MF), Post-polycythemia Vera MF, or Post-essential Thrombocythemia MFPhase 31562023-05-23Primary Myelofibrosis (PMF), Post-polycythemia Vera (Post-PV), Post-essential Thrombocythemia Myelofibrosis (Post-ET MF)MOMELOTINIBIts record names the diseaseClinicalTrials.gov
NCT00509899Open Label Ruxolitinib (INCB018424) in Patients With Myelofibrosis and Post Polycythemia Vera/Essential Thrombocythemia MyelofibrosisPhase 1/21542012-08-02Myelofibrosis, Polycythemia Vera, ThrombocytosisRUXOLITINIBIts record names the diseaseClinicalTrials.gov
NCT00463385A Phase II Study of Pomalidomide in Myelofibrosis With Myeloid MetaplasiaPhase 2882013-10-28Myelofibrosis With Myeloid Metaplasia, Myeloid Metaplasia, MyelofibrosisPOMALIDOMIDE, PREDNISONEIts record names the diseaseClinicalTrials.gov

1 to 10 of 65

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Comparisons in its trials18

Comparisons Trial comparisons calculated in the trials shown here, most participants first. A comparison in one of these trials does not always compare a treatment for the disease, so read the two groups.

ComparisonGroup 1, with the outcomeGroup 2, with the outcomeParticipantsTrialSource
Pacritinib vs Best Available Therapy: Spleen Volume Reduction42 of 2205 of 107327NCT01773187Trial comparisons
Pacritinib vs Best Available Therapy: deaths from any cause27 of 2203 of 106326NCT01773187Trial comparisons
Pacritinib vs Best Available Therapy: serious adverse events117 of 22033 of 106326NCT01773187Trial comparisons
Ruxolitinib vs Placebo: Number of Participants Achieving ≥ 35% Reduction in Spleen Volume From Baseline to Week 2465 of 1551 of 153308NCT00952289Trial comparisons
Ruxolitinib vs Placebo: serious adverse events43 of 15553 of 151306NCT00952289Trial comparisons
Ruxolitinib vs Placebo: Number of Participants With a ≥ 50% Reduction in Total Symptom Score From Baseline to Week 2468 of 1488 of 152300NCT00952289Trial comparisons
Pacritinib vs Best Available Therapy: Total Symptom Score (TSS) Reduction19 of 1005 of 48148NCT01773187Trial comparisons
MMB 200 mg QD + Placebo vs DAN 300 mg BID + Placebo: Number of Baseline TD Participants With TI Status at Week 249 of 633 of 3497NCT04173494Trial comparisons
Treatment Arm vs Observation Arm: deaths from any cause0 of 50 of 38NCT01758588Trial comparisons
Treatment Arm vs Observation Arm: serious adverse events2 of 50 of 38NCT01758588Trial comparisons

Papers from its trials60

The papers the trials shown here list on ClinicalTrials.gov as their results (RESULT) or as drawn from them (DERIVED), results first, newest first.

PMIDListed asTrials listing itSource
30409796RESULT1PubMed
25616577RESULT1PubMed
24038026RESULT1PubMed
23701016RESULT1PubMed
22718840RESULT1PubMed
22375971RESULT1PubMed
20843246RESULT1PubMed
18451242RESULT1PubMed
42855460DERIVED1PubMed
42751490DERIVED1PubMed

Data dates

The date of each source this release read.

Open Targets
2026-09-18
Open Targets
Drug links and their checks, from Drugs and targets
2026-09-18
Drugs and targets
ClinicalTrials.gov, from Trials
2026-11-12
Trials
Comparisons, from Trial comparisons
2026-03-23
Trial comparisons
PubMed, for the checks
2026-11-06
PubMed
MeSH, for the checks
2026-11-10
MeSH

Sources 6

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • NLM's MeSHNLM's terms
  • Open TargetsCC0 1.0
  • PubMedNLM's terms
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • NLM's MeSHNLM's
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PubMedNLM's terms

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this disease from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/diseases/v1/MONDO_0009692

GET https://conductscience.org/api/diseases/v1/MONDO_0009692/drugs?page=2