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Disease ยท MONDO_0007886

uterine corpus leiomyoma

6 sourcesdiseases-2026-09-18-0.1.0

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ConductScience Library. uterine corpus leiomyoma. Diseases, record MONDO_0007886. Release diseases-2026-09-18-0.1.0, 18 Sept 2026. https://conductscience.org/library/diseases/MONDO_0007886

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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
uterine corpus leiomyoma
Open Targets
Open Targets ID
MONDO_0007886
Open Targets
Other names
Benign uterine leiomyomas, Uterine leiomyoma, body of uterus fibroid, body of uterus leiomyoma, corpus uteri fibroid, corpus uteri leiomyoma, fibroid of body of uterus, fibroid of corpus uteri, fibroid of the body of uterus, fibroid of the corpus uteri, fibroid of the uterine body, fibroid of the uterine corpus, fibroid of uterine body, fibroid of uterine corpus, leiomyoma of body of uterus, leiomyoma of corpus uteri, leiomyoma of the body of uterus, leiomyoma of the corpus uteri, leiomyoma of the uterine body, leiomyoma of the uterine corpus, leiomyoma of uterine body, leiomyoma of uterine corpus, plexiform leiomyoma, uterine body fibroid, uterine body leiomyoma, uterine corpus fibroid, uterine corpus leiomyomata, uterine fibroid
Open Targets
Disease Ontology
DOID:13223
Disease Ontology
NCI Thesaurus
C3434
NCI Thesaurus
Highest stage of its drugs
Approval, for 1 of its 40 drugs, from PMDA
Open Targets

Drugs40

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
RELUGOLIXCHEMBL1800159Small moleculeApprovalPMDA1099Drugs and targets
TELAPRISTONE ACETATECHEMBL2105694Small moleculePhase 3ClinicalTrials.gov131313Drugs and targets
NORETHINDRONE ACETATECHEMBL1201146Small moleculePhase 3ClinicalTrials.gov111111Drugs and targets
ESTRADIOLCHEMBL135Small moleculePhase 3ClinicalTrials.gov101010Drugs and targets
ULIPRISTAL ACETATECHEMBL260538Small moleculePhase 3ClinicalTrials.gov101010Drugs and targets
MIFEPRISTONECHEMBL1276308Small moleculePhase 3ClinicalTrials.gov888Drugs and targets
MISOPROSTOLCHEMBL606Small moleculePhase 3ClinicalTrials.gov888Drugs and targets
ASOPRISNILCHEMBL267431Small moleculePhase 3ClinicalTrials.gov777Drugs and targets
VILAPRISANCHEMBL3989936Small moleculePhase 3ClinicalTrials.gov777Drugs and targets
ELAGOLIXCHEMBL1208155Small moleculePhase 3ClinicalTrials.gov and TTD766Drugs and targets

1 to 10 of 40

See all 40 drugs

Targets51

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
GNRHRGonadotropin-releasing hormone receptor10Gonadotropin-releasing hormone receptor agonist; Gonadotropin-releasing hormone receptor antagonistApprovalhttps://conductscience.org/library/genes/2798Drugs and targets
PGRProgesterone receptor8Progesterone receptor agonist; Progesterone receptor antagonist; Progesterone receptor modulatorPhase 3https://conductscience.org/library/genes/5241Drugs and targets
AVPR1AVasopressin V1 receptor2Vasopressin V1 receptor binding agent; Vasopressin receptor agonistUnknownhttps://conductscience.org/library/genes/552Drugs and targets
AVPR1BVasopressin V1 receptor2Vasopressin V1 receptor binding agent; Vasopressin receptor agonistUnknownhttps://conductscience.org/library/genes/553Drugs and targets
AVPR2Vasopressin V2 receptor2Vasopressin V2 receptor binding agent; Vasopressin receptor agonistUnknownhttps://conductscience.org/library/genes/554Drugs and targets
OXTROxytocin receptor2Oxytocin receptor agonistPhase 3https://conductscience.org/library/genes/5021Drugs and targets
PTGER3Prostaglandin E2 receptor2Prostaglandin E2 receptor agonist; Prostanoid EP3 receptor agonistPhase 3https://conductscience.org/library/genes/5733Drugs and targets
ADRA1AAdrenergic receptor1Adrenergic receptor agonistUnknownhttps://conductscience.org/library/genes/148Drugs and targets
ADRA1BAdrenergic receptor1Adrenergic receptor agonistUnknownhttps://conductscience.org/library/genes/147Drugs and targets
ADRA1DAdrenergic receptor1Adrenergic receptor agonistUnknownhttps://conductscience.org/library/genes/146Drugs and targets

1 to 10 of 51

See all 51 targets

Trials103

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. 1 more is not shown, since the checks do not confirm it.

TrialTitlePhaseParticipantsResults first postedConditionsDrugsLinked bySource
NCT03194646Assess Safety and Efficacy of Vilaprisan in Subjects With Uterine FibroidsPhase 31,2722021-08-26Uterine FibroidsVILAPRISANOpen Targets' reading of its recordClinicalTrials.gov
NCT01817530Safety and Efficacy in Premenopausal Women With Heavy Menstrual Bleeding (HMB) Associated With Uterine Fibroids (UF)Phase 25712020-07-21Heavy Uterine Bleeding, Uterine FibroidsELAGOLIX, ESTRADIOL, NORETHINDRONE ACETATEOpen Targets' reading of its recordClinicalTrials.gov
NCT03412890LIBERTY EXTENSION: Efficacy and Safety Extension Study of Relugolix in Women With Heavy Menstrual Bleeding Associated With Uterine FibroidsPhase 34772024-05-09Heavy Menstrual Bleeding, Uterine FibroidESTRADIOL, NORETHINDRONE ACETATE, RELUGOLIXIts record names the diseaseClinicalTrials.gov
NCT01629563PGL4001 Efficacy Assessment in Reduction of Symptoms Due to Uterine LeiomyomataPhase 34512019-09-04Uterine FibroidsULIPRISTAL ACETATEOpen Targets' reading of its recordClinicalTrials.gov
NCT02925494An Extension Study to Evaluate the Efficacy and Safety of Elagolix in Premenopausal Women With Heavy Menstrual Bleeding Associated With Uterine FibroidsPhase 34332020-06-30Uterine Fibroids, Heavy Menstrual BleedingELAGOLIX, ESTRADIOL, NORETHINDRONE ACETATEOpen Targets' reading of its recordClinicalTrials.gov
NCT02654054Efficacy and Safety of Elagolix in Combination With Estradiol/Norethindrone Acetate for the Management of Heavy Menstrual Bleeding Associated With Uterine Fibroids in Premenopausal WomenPhase 34132020-06-29Uterine Fibroids, Heavy Menstrual BleedingELAGOLIX, ESTRADIOL, NORETHINDRONE ACETATEOpen Targets' reading of its recordClinicalTrials.gov
NCT03103087LIBERTY 2: Efficacy & Safety Study of Relugolix in Women With Heavy Menstrual Bleeding Associated With Uterine FibroidsPhase 33822022-04-20Heavy Menstrual Bleeding, Uterine FibroidESTRADIOL, NORETHINDRONE ACETATE, RELUGOLIXIts record names the diseaseClinicalTrials.gov
NCT02691494
Efficacy and Safety of Elagolix in Combination With Estradiol/Norethindrone Acetate for the Management of Heavy Menstrual Bleeding Associated With Uterine Fibroids in Premenopausal Women (Replicate Study)
Phase 33782020-06-30Uterine Fibroids, Heavy Menstrual BleedingELAGOLIX, ESTRADIOL, NORETHINDRONE ACETATEOpen Targets' reading of its recordClinicalTrials.gov
NCT02131662Bay1002670, Fibroids, Safety and Efficacy EU,US,Can, JapPhase 23092017-12-08LeiomyomaVILAPRISANOpen Targets' reading of its recordClinicalTrials.gov
NCT00740831PGL4001 Versus GnRH-agonist in Uterine MyomasPhase 33012012-11-16Uterine MyomasLEUPROLIDE ACETATE, ULIPRISTAL ACETATEOpen Targets' reading of its recordClinicalTrials.gov

1 to 10 of 103

See all 103 trials

Comparisons in its trials22

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
Ulipristal Acetate (PGL4001) 5mg vs Ulipristal Acetate (PGL4001) 10mg: serious adverse events16 of 23012 of 221451NCT01629563Trial comparisons
Relugolix 40 mg vs Leuprorelin 1.88 mg or 3.75 mg: Number of Participants With TEAE Related to Weight0 of 1380 of 142280NCT02655237Trial comparisons
Relugolix 40 mg vs Leuprorelin 1.88 mg or 3.75 mg: Number of Participants With TEAE Related to Standard 12-Lead ECGs0 of 1380 of 142280NCT02655237Trial comparisons
Relugolix 40 mg vs Leuprorelin 1.88 mg or 3.75 mg: Number of Participants Who Had One or More Treatment Emergent Adverse Event (TEAE)131 of 138139 of 142280NCT02655237Trial comparisons
Relugolix 40 mg vs Leuprorelin 1.88 mg or 3.75 mg: deaths from any cause0 of 1380 of 142280NCT02655237Trial comparisons
Relugolix 40 mg vs Leuprorelin 1.88 mg or 3.75 mg: Number of Participants With TEAE (Bone Density Decreased) Related to Bone Mineral Density6 of 1388 of 142280NCT02655237Trial comparisons
Relugolix 40 mg vs Leuprorelin 1.88 mg or 3.75 mg: serious adverse events0 of 1382 of 142280NCT02655237Trial comparisons
Relugolix Plus E2/NETA (Group A) vs Placebo (Group C): Sustained Amenorrhea Rate (No Or Negligible Bleeding)63 of 1254 of 129254NCT03103087Trial comparisons
Relugolix Plus E2/NETA (Group A) vs Placebo (Group C): Number Of Responders With At Least 20 Points Decrease in UFS-QoL Bleeding And Pelvic Discomfort Scale Score79 of 12537 of 129254NCT03103087Trial comparisons
Relugolix Plus E2/NETA (Group A) vs Placebo (Group C): Number Of Responders With At Least 20 Points Increase From Baseline At Week 24 In UFS-QoL Revised Activities Scale Score78 of 12542 of 129254NCT03103087Trial comparisons

Papers from its trials82

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
39084498RESULT1PubMed
38453041RESULT1PubMed
37666383RESULT2PubMed
36989026RESULT1PubMed
36357960RESULT3PubMed
36303616RESULT1PubMed
34741454RESULT1PubMed
33596357RESULT2PubMed
33461754RESULT1PubMed
32532486RESULT1PubMed

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_0007886

GET https://conductscience.org/api/diseases/v1/MONDO_0007886/drugs?page=2