Disease · MONDO_0008159
postmenopausal osteoporosis
6 sourcesdiseases-2026-09-18-0.1.0
Cite this record
ConductScience Library. postmenopausal osteoporosis. Diseases, record MONDO_0008159. Release diseases-2026-09-18-0.1.0, 18 Sept 2026. https://conductscience.org/library/diseases/MONDO_0008159
On this page
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.
- Other names
Bone Loss, Perimenopausal, Bone Loss, Postmenopausal, Bone Losses, Perimenopausal, Bone Losses, Postmenopausal, Osteoporoses, Post-Menopausal, Osteoporoses, Postmenopausal, Osteoporosis, Post Menopausal, Osteoporosis, Postmenopausal, Perimenopausal Bone Loss, Perimenopausal Bone Losses, Post-Menopausal Osteoporoses, Post-Menopausal Osteoporosis, Postmenopausal Bone Loss, Postmenopausal Bone Losses, Postmenopausal Osteoporoses
- Open Targets
- Highest stage of its drugs
- Approval, for 20 of its 24 drugs, from DailyMed, EMA Human Drugs, FDA and TTD
- Open Targets
Drugs24
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.
| Drug | ChEMBL ID | Type | Open Targets' stage | Stage reported by | Reports | Of them trials | Trials shown here | Source |
|---|---|---|---|---|---|---|---|---|
| ALENDRONIC ACID | CHEMBL870 | Small molecule | Approval | EMA Human Drugs | 6 | 3 | 3 | Drugs and targets |
| IBANDRONIC ACID | CHEMBL997 | Small molecule | Approval | EMA Human Drugs | 6 | 3 | 3 | Drugs and targets |
| DENOSUMAB | CHEMBL1237023 | Antibody | Approval | EMA Human Drugs and TTD | 18 | 2 | 2 | Drugs and targets |
| ZOLEDRONIC ACID | CHEMBL4303669 | Small molecule | Approval | DailyMed and EMA Human Drugs | 5 | 2 | 2 | Drugs and targets |
| TERIPARATIDE | CHEMBL525610 | Protein | Approval | EMA Human Drugs | 7 | 1 | 1 | Drugs and targets |
| IBANDRONATE SODIUM | CHEMBL3989569 | Small molecule | Approval | DailyMed | 8 | 0 | 0 | Drugs and targets |
| RISEDRONATE SODIUM | CHEMBL1654 | Small molecule | Approval | DailyMed | 8 | 0 | 0 | Drugs and targets |
| ALENDRONATE SODIUM | CHEMBL675 | Small molecule | Approval | DailyMed and FDA | 6 | 0 | 0 | Drugs and targets |
| BAZEDOXIFENE ACETATE | CHEMBL2106615 | Small molecule | Approval | DailyMed | 3 | 0 | 0 | Drugs and targets |
| CHOLECALCIFEROL | CHEMBL1042 | Small molecule | Approval | EMA Human Drugs | 3 | 0 | 0 | Drugs and targets |
1 to 10 of 24
See all 24 drugsTargets8
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.
| Target | Protein | Its drugs that act on it | Mechanisms | Highest stage of those drugs | Gene in Genes | Source |
|---|---|---|---|---|---|---|
| FDPS | Farnesyl pyrophosphate synthase | 7 | Farnesyl diphosphate synthase inhibitor | Approval | https://conductscience.org/library/genes/2224 | Drugs and targets |
| ESR1 | Estrogen receptor | 6 | Estrogen receptor agonist; Estrogen receptor alpha agonist; Estrogen receptor modulator | Approval | https://conductscience.org/library/genes/2099 | Drugs and targets |
| ESR2 | Estrogen receptor | 5 | Estrogen receptor agonist; Estrogen receptor beta modulator; Estrogen receptor modulator | Approval | https://conductscience.org/library/genes/2100 | Drugs and targets |
| PTH1R | Parathyroid hormone/parathyroid hormone-related peptide receptor | 3 | Parathyroid hormone receptor agonist | Approval | https://conductscience.org/library/genes/5745 | Drugs and targets |
| CALCR | Calcitonin receptor | 2 | Calcitonin receptor agonist | Approval | https://conductscience.org/library/genes/799 | Drugs and targets |
| VDR | Vitamin D3 receptor | 2 | Vitamin D receptor agonist | Approval | https://conductscience.org/library/genes/7421 | Drugs and targets |
| SOST | Sclerostin | 1 | Sclerostin inhibitor | Approval | https://conductscience.org/library/genes/50964 | Drugs and targets |
| TNFSF11 | Tumor necrosis factor ligand superfamily member 11 | 1 | Tumor necrosis factor ligand superfamily member 11 inhibitor | Approval | https://conductscience.org/library/genes/8600 | Drugs and targets |
Trials14
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.
| Trial | Title | Phase | Participants | Results first posted | Conditions | Drugs | Linked by | Source |
|---|---|---|---|---|---|---|---|---|
| NCT00541658 | A Study of a 35 mg Delayed Release Formulation of Risedronate for Osteoporosis | Phase 3 | 923 | 2011-06-21 | Postmenopausal Osteoporosis | RISEDRONIC ACID | Its record names the disease | ClinicalTrials.gov |
| NCT00545779 | BONCURE Study: A Study of Monthly Bonviva (Ibandronate) in Women With Post-Menopausal Osteoporosis on Bisphosphonate Therapy. | Phase 3 | 677 | 2016-10-28 | Post-Menopausal Osteoporosis | IBANDRONIC ACID | Its record names the disease | ClinicalTrials.gov |
| NCT01652690 | Prospective Observational Study to Describe Characteristics and Management of Patients Treated With Denosumab (Prolia®) in Routine Clinical Practice | 600 | 2016-05-26 | Osteoporosis, Postmenopausal | DENOSUMAB | Its record names the disease | ClinicalTrials.gov | |
| NCT00918749 | Delayed Release (DR) Risedronate Compared to Immediate Release (IR) in Postmenopausal Women | Phase 2 | 205 | 2011-03-24 | Postmenopausal Osteoporosis | RISEDRONIC ACID | Its record names the disease | ClinicalTrials.gov |
| NCT00577720 | Assess the Safety, Efficacy, and Pharmacokinetics of Immediate and Delayed Release Weekly Risedronate | Phase 2 | 181 | 2012-01-13 | Postmenopausal Women | RISEDRONIC ACID | Its record names the disease | ClinicalTrials.gov |
| NCT00361595 | Intervenous (IV) Zoledronic Acid After Forteo in Postmenopausal Women | Not applicable | 35 | 2011-01-14 | Osteoporosis | ZOLEDRONIC ACID | Its record names the disease | ClinicalTrials.gov |
| NCT01128257 | A Study of Ibandronate [Bonviva/Boniva] and Alendronate in Female Patients With Post-Menopausal Osteoporosis | 6,054 | Postmenopausal Osteoporosis | ALENDRONIC ACID, IBANDRONIC ACID | Its record names the disease | ClinicalTrials.gov | ||
| NCT00666627 | Bisphosphonate Action on the Appendicular Skeleton: Evidence for Differential Effects | Phase 2 | 410 | Post-menopausal Osteoporosis | ALENDRONIC ACID, IBANDRONIC ACID, RISEDRONIC ACID | Its record names the disease | ClinicalTrials.gov | |
| NCT01155232 | Effects of Teriparatide (PTH) on Bone in Men and Women With Osteoporosis | 100 | Osteoporosis | TERIPARATIDE | Its record names the disease | ClinicalTrials.gov | ||
| NCT04702204 | Efficacy of Denosumab Treatment in Bisphosphonate Unresponsive Patients | 73 | Postmenopausal Osteoporosis | DENOSUMAB | Its record names the disease | ClinicalTrials.gov |
1 to 10 of 14
See all 14 trialsComparisons in its trials2
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.
| Comparison | Group 1, with the outcome | Group 2, with the outcome | Participants | Trial | Source |
|---|---|---|---|---|---|
| Czech Republic vs Slovakia: Number of Participants Receiving All Prescriptions and Injections of Denosumab From the Initial Prescribing Physician's Office | 295 of 300 | 296 of 300 | 600 | NCT01652690 | Trial comparisons |
| Czech Republic vs Slovakia: serious adverse events | 0 of 300 | 1 of 300 | 600 | NCT01652690 | Trial comparisons |
Papers from its trials1
The papers the trials shown here list on ClinicalTrials.gov as their results (RESULT) or as drawn from them (DERIVED), results first, newest first.
| PMID | Listed as | Trials listing it |
|---|---|---|
| 21947137 | DERIVED | 1 |
Source PubMed
Data dates
The date of each source this release read.
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_0008159
GET https://conductscience.org/api/diseases/v1/MONDO_0008159/drugs?page=2