Bazedoxifene Acetate
FDA-approved product (tablet, oral).
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Postmenopausal osteoporosis
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Selective estrogen receptor modulators
- Anti-infective classification
- Not classified as an anti-infective.
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against M. tuberculosis, MRSA and E. coli. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA51.9% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli43.1% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae29.6% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis61.4% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
A model’s estimate of laboratory activity against each pathogen species. It is not clinical effectiveness.
Evidence
Clinical and experimental
Documented evidenceClinical
50+registered studies name this medicine, for any condition. The registry search keeps the first 50, so there may be more. See them below.
Experimental
No evidence found
No laboratory measurement against the four pathogens in the ChEMBL records loaded here.
Docking
Computational · nothing measuredDihydrofolate reductase ↗ (E. coli)
Not yet docked: queued in the docking rundetails
KPC-2 carbapenemase ↗ (K. pneumoniae)
Not yet docked: queued in the docking rundetails
Enoyl-ACP reductase (InhA) ↗ (M. tuberculosis)
Not yet docked: queued in the docking rundetails
Dihydrofolate reductase ↗ (MRSA)
Not yet docked: queued in the docking rundetails
AutoDock Vina, one experimentally solved protein per pathogen. This project’s screening target is -7.0 kcal/mol, its own mark rather than a universal cutoff. A docking score is a structural hypothesis, not proof of binding, and requires experimental validation.
Other medicines to investigate
AI prediction · nothing measuredOther repurposing candidates: approved medicines besides Bazedoxifene Acetate with AI-predicted activity ≥40% against the chosen pathogen, leaving out existing antimicrobials. They are computational candidates for further investigation, not alternatives and not recommendations.
Sorted by AI-predicted activity, high to low. The order is not a ranking of which medicine is better.
- Mefloquine HydrochlorideExisting use: Malaria, Plasmodium falciparum malaria, Plasmodium vivax malaria81.8% AI-predicted activityagainst M. tuberculosisLab records exist8 registered studies
- KetoconazoleExisting use: Adrenal gland disease, Blastomycosis, Cushing syndrome and 3 more81.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- LevoketoconazoleExisting use: Adrenal gland disease, Adrenal gland hyperfunction, Cushing syndrome81.2% AI-predicted activityagainst M. tuberculosis6 registered studies
- Fluphenazine DecanoateExisting use: Mental or behavioural disorder, Psychosis80.7% AI-predicted activityagainst M. tuberculosis4 registered studies
- Fluphenazine EnanthateExisting use: Mental or behavioural disorder, Psychosis80.7% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- NifurtimoxExisting use: American trypanosomiasis, Chagas disease, Leishmaniasis and 1 more78.4% AI-predicted activityagainst M. tuberculosis19 registered studies
- Fluphenazine HydrochlorideExisting use: Mental or behavioural disorder, Psychosis77.8% AI-predicted activityagainst M. tuberculosis5 registered studies
- NitazoxanideExisting use: Amebiasis, Diarrhea77.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- TopiramateExisting use: Epilepsy, Lennox-Gastaut syndrome, Migraine disorder and 1 more77.4% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- TrabectedinExisting use: Cancer, Dedifferentiated liposarcoma, Leiomyosarcoma and 7 more76.8% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Chlorpromazine HydrochlorideExisting use: Conduct disorder, Mental or behavioural disorder, Nausea and vomiting and 3 more75.0% AI-predicted activityagainst M. tuberculosis33 registered studies
- ProchlorperazineExisting use: Anxiety disorder, Nausea and vomiting, Psychosis and 1 more74.1% AI-predicted activityagainst M. tuberculosis50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Affect of Duavive on Mood & Anxiety Symptoms
NCT04478305 · start 2024-07-03
Registered record
- Registry ID
- NCT04478305
- Conditions
- Menopause; Depression, Anxiety; Sleep; Menopause Related Conditions
- Interventions
- Duavive 0.45Mg-20Mg Tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Recruiting
- Start
- 2024-07-03
- Completion
- 2025-12
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMenopause; Depression, Anxiety; Sleep; Menopause Related ConditionsInterventionDuavive 0.45Mg-20Mg TabletPhasePhase 1Registry statusRecruitingEffects of Novel Estrogens on Glucose and Lipids in Postmenopausal Prediabetic Women Veterans
NCT05073237 · start 2024-04-08
Registered record
- Registry ID
- NCT05073237
- Conditions
- Menopause; Prediabetes; Obesity
- Interventions
- Placebo; conjugated estrogens/bazedoxifene (CE/BZA)
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Withdrawn
- Start
- 2024-04-08
- Completion
- 2024-04-08
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMenopause; Prediabetes; ObesityInterventionPlacebo; conjugated estrogens/bazedoxifene (CE/BZA)PhasePhase 2Registry statusWithdrawnEndometriosis and Microvascular Dysfunction; Simvastatin and Duavee
NCT05059626 · start 2023-12-01
Registered record
- Registry ID
- NCT05059626
- Conditions
- Endometriosis
- Interventions
- simvastatin 10mg; Bazedoxifene 20/Estrogens,Con 0.45Mg Tb
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Enrolling by invitation
- Start
- 2023-12-01
- Completion
- 2026-12-31
- Enrolment
- 28
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEndometriosisInterventionsimvastatin 10mg; Bazedoxifene 20/Estrogens,Con 0.45Mg TbPhasePhase 4Registry statusEnrolling by invitationBazedoxifene as a Concomitant Treatment of Patients With Metastatic Pancreatic Adenocarcinoma
NCT04812808 · start 2022-02-01
Registered record
- Registry ID
- NCT04812808
- Conditions
- Pancreas Cancer
- Interventions
- Bazedoxifene 20 mg
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2022-02-01
- Completion
- 2024-05-31
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPancreas CancerInterventionBazedoxifene 20 mgPhaseNot applicableRegistry statusUnknownPhase IIB Trial of Bazedoxifene Plus Conjugated Estrogens
NCT04821141 · start 2021-12-14
Registered record
- Registry ID
- NCT04821141
- Conditions
- Risk Reduction; Breast Cancer
- Interventions
- Bazedoxifene and Conjugated Estrogens
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Active not recruiting
- Start
- 2021-12-14
- Completion
- 2027-07-31
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRisk Reduction; Breast CancerInterventionBazedoxifene and Conjugated EstrogensPhasePhase 2Registry statusActive not recruitingPilot Study of Bazedoxifene Plus Conjugated Estrogen on Imaging and Blood Biomarkers
NCT04821375 · start 2021-12-02
Registered record
- Registry ID
- NCT04821375
- Conditions
- Increased Risk for Development of Breast Cancer
- Interventions
- bazedoxifene plus conjugated estrogens
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Completed
- Start
- 2021-12-02
- Completion
- 2024-12-31
- Enrolment
- 16
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionIncreased Risk for Development of Breast CancerInterventionbazedoxifene plus conjugated estrogensPhaseEarly phase 1Registry statusCompletedAdvancing Postmenopausal Preventive Therapy
NCT04103476 · start 2021-04-13
Registered record
- Registry ID
- NCT04103476
- Conditions
- Atherosclerosis; Cognitive Decline
- Interventions
- Oral bazedoxifene 20 mg / conjugated estrogens 0.45 mg; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Active not recruiting
- Start
- 2021-04-13
- Completion
- 2026-12-31
- Enrolment
- 385
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAtherosclerosis; Cognitive DeclineInterventionOral bazedoxifene 20 mg / conjugated estrogens 0.45 mg; PlaceboPhasePhase 2Registry statusActive not recruitingPost-fracture Medication and Mortality
NCT05366621 · start 2020-11-01
Registered record
- Registry ID
- NCT05366621
- Conditions
- Osteoporosis; Osteoporosis Fracture; Drug Therapy; Mortality; Adherence, Medication
- Interventions
- Anti-osteoporosis medications
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2020-11-01
- Completion
- 2021-10-31
- Enrolment
- 216,155
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOsteoporosis; Osteoporosis Fracture; Drug Therapy; Mortality +1 moreInterventionAnti-osteoporosis medicationsPhaseNot recordedRegistry statusCompletedPilot Study of Effects of Duavee® on Imaging and Blood Biomarkers In Women With Menopausal Symptoms
NCT04379024 · start 2020-06-01
Registered record
- Registry ID
- NCT04379024
- Conditions
- Focus of Study is Healthy Women at Risk for Breast Cancer
- Interventions
- DUAVEE 0.45Mg-20Mg Tablet
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Terminated
- Start
- 2020-06-01
- Completion
- 2021-07-31
- Enrolment
- 11
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionFocus of Study is Healthy Women at Risk for Breast CancerInterventionDUAVEE 0.45Mg-20Mg TabletPhaseEarly phase 1Registry statusTerminatedBazedoxifene Acetate as a Remyelinating Agent in Multiple Sclerosis
NCT04002934 · start 2019-09-10
Registered record
- Registry ID
- NCT04002934
- Conditions
- Multiple Sclerosis; Multiple Sclerosis, Relapsing-Remitting
- Interventions
- Bazedoxifene Acetate
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2019-09-10
- Completion
- 2025-05-20
- Enrolment
- 63
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMultiple Sclerosis; Multiple Sclerosis, Relapsing-RemittingInterventionBazedoxifene AcetatePhasePhase 2Registry statusCompletedCan we Use Estrogen-containing Therapy to Improve Pain in Women After Menopause With Hand Osteoarthritis?
NCT04036929 · start 2019-05-09
Registered record
- Registry ID
- NCT04036929
- Conditions
- Hand Osteoarthritis
- Interventions
- Estrogen-bazedoxifene; Placebo oral tablet
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2019-05-09
- Completion
- 2021-12-10
- Enrolment
- 28
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHand OsteoarthritisInterventionEstrogen-bazedoxifene; Placebo oral tabletPhaseNot applicableRegistry statusCompletedEffects of a Tissue Selective Estrogen Complex (TSEC) on Depression and the Neural Reward System in the Perimenopause"
NCT03740009 · start 2019-01-02
Registered record
- Registry ID
- NCT03740009
- Conditions
- Perimenopausal Disorder; Depression
- Interventions
- Bazedoxifene/Conjugated Estrogen
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2019-01-02
- Completion
- 2021-05-17
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPerimenopausal Disorder; DepressionInterventionBazedoxifene/Conjugated EstrogenPhasePhase 4Registry statusCompletedA Clinical Trial to Evaluate the Safety and Pharmacokinetic
NCT03475719 · start 2018-01-11
Registered record
- Registry ID
- NCT03475719
- Conditions
- Osteoporosis, Postmenopausal
- Interventions
- HUG186-B and HUG186-D; HUG186
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Unknown
- Start
- 2018-01-11
- Completion
- 2018-04-30
- Enrolment
- 52
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOsteoporosis, PostmenopausalInterventionHUG186-B and HUG186-D; HUG186PhasePhase 1Registry statusUnknownHDDO-1614 Bio Equivalence Study
NCT03382314 · start 2017-10-16
Registered record
- Registry ID
- NCT03382314
- Conditions
- Osteoporosis
- Interventions
- HDDO-1614; Bazedoxifene / Cholecalciferol
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2017-10-16
- Completion
- 2018-01-05
- Enrolment
- 38
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOsteoporosisInterventionHDDO-1614; Bazedoxifene / CholecalciferolPhasePhase 1Registry statusCompletedAK-R215 Pharmacokinetic Study Phase I
NCT03321318 · start 2017-07-13
Registered record
- Registry ID
- NCT03321318
- Conditions
- Healthy
- Interventions
- AK-R215; Bazedoxifene 20 mg; Cholecalciferol 800IU
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Unknown
- Start
- 2017-07-13
- Completion
- 2018-01-12
- Enrolment
- 52
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionAK-R215; Bazedoxifene 20 mg; Cholecalciferol 800IUPhasePhase 1Registry statusUnknown