Tenofovir Alafenamide Fumarate
FDA-approved product (tablet, oral), marketed as Tenofovir Alafenamide, Tenofovir Alafenamide Fumarate, Vemlidy.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Chronic hepatitis B virus infection
- Hepatitis B virus infection
- HIV infection
- HIV-1 infection
- Viral disease
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Nucleoside and nucleotide reverse transcriptase inhibitors
- Anti-infective classification
- Classified as another kind of anti-infective (for example an antifungal, antiviral or antiparasitic medicine).WHO ATC J05AF13
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against E. coli and M. tuberculosis. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA35.1% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- E. coli42.3% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae20.9% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis61.6% 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 Tenofovir Alafenamide Fumarate 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.
Clinical Trial of TQA3605 Tablet in Combination With Nucleos(t)Ide Analogues(NAs) Versus NAs Alone for the Treatment of Patients With Chronic Hepatitis B Virus Infection Who Have Undergone Treatment and Exhibit Low Viral Load or Poor Response
NCT07797231 · start 2026-09
Registered record
- Registry ID
- NCT07797231
- Conditions
- Chronic Hepatitis B
- Interventions
- TQA3605 tablets Placebo; TQA3605 tablets; Entecavir dispersible tablets; Tenofovir Disoproxil Fumarate Tablets; Tenofovir Alafenamide Fumarate Tablets; Tenofovir Amibufenamide Tablets
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Not yet recruiting
- Start
- 2026-09
- Completion
- 2029-10
- Enrolment
- 930
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Hepatitis BInterventionTQA3605 tablets Placebo; TQA3605 tablets; Entecavir dispersible tablets; Tenofovir Disoproxil Fumarate Tablets +2 morePhasePhase 3Registry statusNot yet recruitingStrengthening Hepatitis B Screening, Linkage to Care and Long-Term Monitoring in Phichit Province, Thailand: A Birth Bohort Approach
NCT07258251 · start 2026-01-01
Registered record
- Registry ID
- NCT07258251
- Conditions
- Chronic Hepatitis B; Hepatitis B Virus Infection
- Interventions
- Tenofovir Alafenamide (TAF); Community-Based Support; Simplified WHO 2024 Criteria
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Not yet recruiting
- Start
- 2026-01-01
- Completion
- 2028-12-31
- Enrolment
- 6,000
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Hepatitis B; Hepatitis B Virus InfectionInterventionTenofovir Alafenamide (TAF); Community-Based Support; Simplified WHO 2024 CriteriaPhasePhase 4Registry statusNot yet recruitingA Study to Provide Continued Access to Study Drug to Children and Adolescents Who Have Completed Clinical Studies Involving Gilead HIV Treatments
NCT06337032 · start 2024-08-27
Registered record
- Registry ID
- NCT06337032
- Conditions
- HIV-1-infection
- Interventions
- F/TAF (High Dose Tablet); F/TAF (Low Dose Tablet); F/TAF (Lowest Dose Tablet); F/TAF (High Dose TOS); F/TAF (Low Dose TOS); F/TAF (Lowest Dose TOS); E/C/F/TAF; E/C/F/TAF (Low Dose); Cobicistat (High Dose); Cobicistat (Low Dose); Cobicistat (TOS); B/F/TAF (High Dose); B/F/TAF (Low Dose); B/F/TAF (High Dose TOS); B/F/TAF (Low Dose TOS); B/F/TAF (Lowest Dose TOS); 3rd ARV Agent; Nucleos(t)ide reverse transcriptase inhibitors (NRTI); ATV; DRV; Lopinavir Boosted with ritonavir (LPV/r)
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2024-08-27
- Completion
- 2034-03
- Enrolment
- 350
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV-1-infectionInterventionF/TAF (High Dose Tablet); F/TAF (Low Dose Tablet); F/TAF (Lowest Dose Tablet); F/TAF (High Dose TOS) +17 morePhasePhase 4Registry statusRecruitingObservation Study on Reducing the Risk of Liver Cancer Associated With Hepatitis B (Zhiyuan) Project.
NCT07169656 · start 2024-06-03
Registered record
- Registry ID
- NCT07169656
- Conditions
- Chronic Hepatitis b
- Interventions
- ETV,TDF,TAF,TMF; Peginterferon α-2b injection
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Recruiting
- Start
- 2024-06-03
- Completion
- 2032-12-31
- Enrolment
- 15,000
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Hepatitis bInterventionETV,TDF,TAF,TMF; Peginterferon α-2b injectionPhaseNot recordedRegistry statusRecruitingClinical Trial for Non-inferiority and Safety of Tenofovir Alafenamide and Tenofovir Disoproxil Fumarate in Patients With Hematologic Malignancies Who Require Prophylactic Hepatitis B Antiviral Treatment
NCT06221657 · start 2024-02-01
Registered record
- Registry ID
- NCT06221657
- Conditions
- Patients With Malignant Blood Disease Requiring Hepatitis B Antiviral Medication
- Interventions
- Vemlidy; Virreal
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Not yet recruiting
- Start
- 2024-02-01
- Completion
- 2026-12-31
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPatients With Malignant Blood Disease Requiring Hepatitis B Antiviral MedicationInterventionVemlidy; VirrealPhasePhase 4Registry statusNot yet recruitingSingle Ascending Dose, Food Effects and Drug-Drug Interactions of ACC017 Tablets in Healthy Adult Participants
NCT06278389 · start 2024-01-24
Registered record
- Registry ID
- NCT06278389
- Conditions
- Healthy Adult Participants
- Interventions
- ACC017 tablets; Emtricitabine and Tenofovir Alafenamide Fumarate Tablets
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2024-01-24
- Completion
- 2024-05-20
- Enrolment
- 48
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthy Adult ParticipantsInterventionACC017 tablets; Emtricitabine and Tenofovir Alafenamide Fumarate TabletsPhasePhase 1Registry statusCompletedThe Effect Tenofovir Disoproxil Fumarate (TDF) and Tenofovir Alafenamide (TAF) on Small Intestine Gut Wall
NCT05326971 · start 2023-01-19
Registered record
- Registry ID
- NCT05326971
- Conditions
- HIV Infections; Weight Gain
- Interventions
- gastroscopy
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2023-01-19
- Completion
- 2025-06-01
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV Infections; Weight GainInterventiongastroscopyPhasePhase 4Registry statusUnknownDoravirine and Weight Gain in Antiretroviral Naive
NCT05457530 · start 2022-08-01
Registered record
- Registry ID
- NCT05457530
- Conditions
- Body Weight Changes; Human Immunodeficiency Virus; ART; Obesity; Minority Health; BMD; Metabolic Syndrome; Fasting
- Interventions
- DOR/3TC/TDF; DOR + FTC/TAF; BIC/FTC/TAF
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Withdrawn
- Start
- 2022-08-01
- Completion
- 2023-05-03
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBody Weight Changes; Human Immunodeficiency Virus; ART; Obesity +4 moreInterventionDOR/3TC/TDF; DOR + FTC/TAF; BIC/FTC/TAFPhasePhase 3Registry statusWithdrawnA Single and Multiple Ascending Dose Study of JNJ-64457744
NCT05423106 · start 2022-07-04
Registered record
- Registry ID
- NCT05423106
- Conditions
- Healthy; Hepatitis B, Chronic
- Interventions
- JNJ-64457744; Placebo; Tenofovir Disoproxil Fumarate (TDF); Tenofovir Alafenamide (TAF); Entecavir (ETV); JNJ-64457744
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Terminated
- Start
- 2022-07-04
- Completion
- 2023-03-20
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthy; Hepatitis B, ChronicInterventionJNJ-64457744; Placebo; Tenofovir Disoproxil Fumarate (TDF); Tenofovir Alafenamide (TAF) +2 morePhasePhase 1Registry statusTerminatedA Follow-up Study of Peginterferon Alfa-2b Combined With TDF in Patients With Chronic Hepatitis B
NCT06707922 · start 2022-03-18
Registered record
- Registry ID
- NCT06707922
- Conditions
- Chronic Hepatitis B
- Interventions
- Peginterferon α-2b Injection; Tenofovir Alafenamide Fumarate
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Enrolling by invitation
- Start
- 2022-03-18
- Completion
- 2029-07-31
- Enrolment
- 350
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Hepatitis BInterventionPeginterferon α-2b Injection; Tenofovir Alafenamide FumaratePhaseNot applicableRegistry statusEnrolling by invitationINSTI's For The Management of HIV-associated TB
NCT04734652 · start 2022-02-18
Registered record
- Registry ID
- NCT04734652
- Conditions
- HIV/AIDS; Tuberculosis, Pulmonary
- Interventions
- Biktarvy®; TLD- fixed-drug combination single tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2022-02-18
- Completion
- 2024-08-31
- Enrolment
- 122
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV/AIDS; Tuberculosis, PulmonaryInterventionBiktarvy®; TLD- fixed-drug combination single tabletPhasePhase 2Registry statusCompletedPeginterferon Treatment Study for Inactive Chronic Hepatitis B Patients
NCT05182463 · start 2022-01-08
Registered record
- Registry ID
- NCT05182463
- Conditions
- Hepatitis B, Chronic
- Interventions
- Peginterferon Alfa-2B; Nucleoside Analogs
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2022-01-08
- Completion
- 2029-11-30
- Enrolment
- 5,000
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis B, ChronicInterventionPeginterferon Alfa-2B; Nucleoside AnalogsPhasePhase 4Registry statusRecruitingEfficacy and Safety Study of Peginterferon Alfacon-2 to Treat Chronic Hepatitis B Virus Infection
NCT06544551 · start 2021-12-28
Registered record
- Registry ID
- NCT06544551
- Conditions
- Chronic Hepatitis B Virus Infection
- Interventions
- Peginterferon Alfacon-2; Peginterferon Alfacon-2 placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2021-12-28
- Completion
- 2023-12-30
- Enrolment
- 336
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Hepatitis B Virus InfectionInterventionPeginterferon Alfacon-2; Peginterferon Alfacon-2 placeboPhasePhase 3Registry statusCompletedSwitching From TDF-based Antiretroviral Therapy Regimens to B/F/TAF in Virally Suppressed Adults With HIV-1 Infection
NCT05122754 · start 2021-12-08
Registered record
- Registry ID
- NCT05122754
- Conditions
- HIV-1-infection
- Interventions
- B/F/TAF; TDF-based triple ART regimen switching to B/F/TAF
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2021-12-08
- Completion
- 2024-04-28
- Enrolment
- 150
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV-1-infectionInterventionB/F/TAF; TDF-based triple ART regimen switching to B/F/TAFPhasePhase 4Registry statusUnknownPre-Exposure Prophylaxis Study of Lenacapavir and Emtricitabine/Tenofovir Alafenamide in Adolescent Girls and Young Women at Risk of HIV Infection
NCT04994509 · start 2021-08-30
Registered record
- Registry ID
- NCT04994509
- Conditions
- Pre-Exposure Prophylaxis of HIV Infection
- Interventions
- Oral Lenacapavir (LEN); Subcutaneous (SC) Lenacapavir (LEN); F/TAF; F/TDF; Placebo SC LEN; PTM Oral LEN; PTM F/TAF; PTM F/TDF
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Active not recruiting
- Start
- 2021-08-30
- Completion
- 2028-01
- Enrolment
- 5,368
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPre-Exposure Prophylaxis of HIV InfectionInterventionOral Lenacapavir (LEN); Subcutaneous (SC) Lenacapavir (LEN); F/TAF; F/TDF +4 morePhasePhase 3Registry statusActive not recruiting