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Disease · MONDO_0004880

bowel dysfunction

6 sourcesdiseases-2026-09-18-0.1.0

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ConductScience Library. bowel dysfunction. Diseases, record MONDO_0004880. Release diseases-2026-09-18-0.1.0, 18 Sept 2026. https://conductscience.org/library/diseases/MONDO_0004880

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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
bowel dysfunction
Open Targets
Open Targets ID
MONDO_0004880
Open Targets
Other names
disease of lower digestive tract, lower digestive tract disease
Open Targets
Disease Ontology
DOID:9779
Disease Ontology
Highest stage of its drugs
Phase 3, for 3 of its 6 drugs, from ClinicalTrials.gov
Open Targets

Drugs6

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
LUBIPROSTONECHEMBL1201134Small moleculePhase 3ClinicalTrials.gov333Drugs and targets
ALVIMOPANCHEMBL270190Small moleculePhase 3ClinicalTrials.gov222Drugs and targets
RIFAXIMINCHEMBL1617Small moleculePhase 3ClinicalTrials.gov111Drugs and targets
BOTULINUM TOXIN TYPE ACHEMBL4297862ProteinPhase 2ClinicalTrials.gov111Drugs and targets
LIDOCAINECHEMBL79Small moleculePhase 2ClinicalTrials.gov111Drugs and targets
METHYLNALTREXONE BROMIDECHEMBL1201770Small moleculePhase 2ClinicalTrials.gov111Drugs and targets

Targets13

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
OPRM1Mu-type opioid receptor2Mu opioid receptor antagonistPhase 3https://conductscience.org/library/genes/4988Drugs and targets
CLCN2Chloride channel protein 21Chloride channel protein 2 openerPhase 3https://conductscience.org/library/genes/1181Drugs and targets
SCN10ASodium channel alpha subunit1Sodium channel alpha subunit blockerPhase 2https://conductscience.org/library/genes/6336Drugs and targets
SCN11ASodium channel alpha subunit1Sodium channel alpha subunit blockerPhase 2https://conductscience.org/library/genes/11280Drugs and targets
SCN1ASodium channel alpha subunit1Sodium channel alpha subunit blockerPhase 2https://conductscience.org/library/genes/6323Drugs and targets
SCN2ASodium channel alpha subunit1Sodium channel alpha subunit blockerPhase 2https://conductscience.org/library/genes/6326Drugs and targets
SCN3ASodium channel alpha subunit1Sodium channel alpha subunit blockerPhase 2https://conductscience.org/library/genes/6328Drugs and targets
SCN4ASodium channel alpha subunit1Sodium channel alpha subunit blockerPhase 2https://conductscience.org/library/genes/6329Drugs and targets
SCN5ASodium channel alpha subunit1Sodium channel alpha subunit blockerPhase 2https://conductscience.org/library/genes/6331Drugs and targets
SCN7ASodium channel alpha subunit1Sodium channel alpha subunit blockerPhase 2https://conductscience.org/library/genes/6332Drugs and targets

1 to 10 of 13

See all 13 targets

Trials9

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
NCT00620061Opioid-induced Bowel Dysfunction: Long-Term Assessment of LubiprostonePhase 34392019-12-30Opioid-Induced Bowel DysfunctionLUBIPROSTONEIts record names the diseaseClinicalTrials.gov
NCT01298219Opioid-induced Bowel Dysfunction (OBD) Pivotal Assessment of Lubiprostone (OPAL)Phase 34392019-12-24Opioid-induced Bowel DysfunctionLUBIPROSTONEIts record names the diseaseClinicalTrials.gov
NCT00597428Opioid-induced Bowel Dysfunction Pivotal Assessment of LubiprostonePhase 34372015-12-07Opioid-Induced Bowel DysfunctionLUBIPROSTONEIts record names the diseaseClinicalTrials.gov
NCT01345175Rifaximin and Placebo in the Treatment of Bowel Dysfunction After Anterior Resection for Rectal CancerPhase 3692024-05-14Rectal CancerRIFAXIMINIts record names the diseaseClinicalTrials.gov
NCT00241722Long-Term Safety Evaluation Of Treatment Of Constipation Due To Opioids Being Taken For Persistent Non-Cancer PainPhase 3805Bowel Dysfunction, ConstipationALVIMOPANIts record names the diseaseClinicalTrials.gov
NCT00259922Alvimopan For The Treatment Of Constipation Due To Opioids Being Taken For Persistent Non-Cancer PainPhase 3485Bowel Dysfunction, ConstipationALVIMOPANIts record names the diseaseClinicalTrials.gov
NCT00366431Study Evaluating Oral MOA-728 for the Treatment of Opioid-Induced Bowel Dysfunction (OIBD) in Subjects With Chronic Non-Malignant PainPhase 2420ConstipationMETHYLNALTREXONE BROMIDEIts record names the diseaseClinicalTrials.gov
NCT01155440Bowel Function After Laparoscopic Colon Surgery: Effect of IV LidocainePhase 260Colon Cancer, Inflammatory Bowel Diseases, DiverticulitisLIDOCAINEIts record names the diseaseClinicalTrials.gov
NCT04991688A Prospective Pilot Study to Assess the Efficacy of BOTOX-A in Patients With Low Anterior Resection Syndrome (LARS>20) and Refractory Medical Treatment After Rectal ResectionPhase 211Low Anterior Resection Syndrome (LARS>20), Refractory Medical Treatment After Rectal ResectionBOTULINUM TOXIN TYPE AIts record names the diseaseClinicalTrials.gov

Comparisons in its trials7

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
Lubiprostone vs Placebo: Number of Participants Classified as Treatment Responders Within 12 Weeks59 of 21941 of 220439NCT01298219Trial comparisons
Lubiprostone vs Placebo: deaths from any cause1 of 2190 of 220439NCT01298219Trial comparisons
Lubiprostone vs Placebo: serious adverse events7 of 2196 of 220439NCT01298219Trial comparisons
Lubiprostone vs Placebo: serious adverse events7 of 2237 of 214437NCT00597428Trial comparisons
Lubiprostone vs Placebo: Responder Rate108 of 223100 of 212435NCT00597428Trial comparisons
Arm 1: Experimental: Pts Receiving Rifaximin vs Arm 2: Placebo Comparator: Pts Receiving Placebo: deaths from any cause0 of 360 of 3369NCT01345175Trial comparisons
Arm 1: Experimental: Pts Receiving Rifaximin vs Arm 2: Placebo Comparator: Pts Receiving Placebo: serious adverse events0 of 361 of 3369NCT01345175Trial comparisons

Papers from its trials2

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
21292168RESULT1PubMed
21519309DERIVED1PubMed

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_0004880

GET https://conductscience.org/api/diseases/v1/MONDO_0004880/drugs