Ertugliflozin
FDA-approved product (tablet, oral), marketed as Ertugliflozin, Steglatro.
- Registered studies
- 49
- Lab records
- 0
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLNo approved indication recorded
ChEMBL records no approved indication for Ertugliflozin. Its therapeutic class is shown instead.
- WHO therapeutic group
- Sodium-glucose co-transporter 2 (sglt2) inhibitors
- 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 and MRSA. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA57.1% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli28.3% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae17.2% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis43.9% 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
49registered studies name this medicine, for any condition. See them below.
Experimental
No evidence found
No laboratory measurement against the four pathogens in the ChEMBL records loaded here.
Docking
Computational · nothing measuredAutoDock 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 Ertugliflozin 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.
Study Of Safety And Efficacy Of Ertugliflozin (PF-04971729, MK-8835) In Participants With Type 2 Diabetes (MK-8835-016)
NCT01059825 · start 2010-02-24
Registered record
- Registry ID
- NCT01059825
- Conditions
- Diabetes Mellitus, Type 2
- Interventions
- Placebo to Ertugliflozin; Ertugliflozin 1 mg; Ertugliflozin 5 mg; Ertugliflozin 25 mg; Sitagliptin 100 mg; Placebo to Sitagliptin; Metformin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2010-02-24
- Completion
- 2011-01-20
- Enrolment
- 375
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDiabetes Mellitus, Type 2InterventionPlacebo to Ertugliflozin; Ertugliflozin 1 mg; Ertugliflozin 5 mg; Ertugliflozin 25 mg +3 morePhasePhase 2Registry statusCompletedEffects of Once and Twice Daily Dosing Regimen of Ertugliflozin (PF-04971729, MK-8835) In Participants With Type 2 Diabetes (MK-8835-040)
NCT01054300 · start 2010-02-17
Registered record
- Registry ID
- NCT01054300
- Conditions
- Diabetes Mellitus, Type 2; Adult
- Interventions
- Ertugliflozin 2 mg single dose; Ertugliflozin 2 mg split into twice daily; Ertugliflozin 4 mg single dose; Ertugliflozin 4 mg split into twice daily; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2010-02-17
- Completion
- 2010-04-07
- Enrolment
- 52
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDiabetes Mellitus, Type 2; AdultInterventionErtugliflozin 2 mg single dose; Ertugliflozin 2 mg split into twice daily; Ertugliflozin 4 mg single dose; Ertugliflozin 4 mg split into twice daily +1 morePhasePhase 1Registry statusCompletedA Multiple Dose Study Of Ertugliflozin (PF-04971729, MK-8835) In Otherwise Healthy Overweight And Obese Volunteers (MK-8835-037)
NCT01018823 · start 2009-12-14
Registered record
- Registry ID
- NCT01018823
- Conditions
- Healthy Volunteer
- Interventions
- Ertugliflozin; Placebo to Ertugliflozin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2009-12-14
- Completion
- 2010-03-18
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthy VolunteerInterventionErtugliflozin; Placebo to ErtugliflozinPhasePhase 1Registry statusCompletedA Single Escalating Dose Study Of Ertugliflozin (PF-04971729, MK-8835) Under Fed and Fasted Conditons In Healthy Volunteers (MK-8835-036)
NCT00989079 · start 2009-10-16
Registered record
- Registry ID
- NCT00989079
- Conditions
- Type 2 Diabetes Mellitus
- Interventions
- Ertugliflozin; Placebo to Ertugliflozin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2009-10-16
- Completion
- 2009-12-11
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionType 2 Diabetes MellitusInterventionErtugliflozin; Placebo to ErtugliflozinPhasePhase 1Registry statusCompleted