Doravirine
FDA-approved product (tablet, oral), marketed as Pifeltro.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- HIV infection
- HIV-1 infection
- Viral disease
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Non-nucleoside reverse transcriptase inhibitors
- FDA pharmacologic class
- Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor FDA label ↗
- Anti-infective classification
- Classified as another kind of anti-infective (for example an antifungal, antiviral or antiparasitic medicine).WHO ATC J05AG06
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against MRSA 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- MRSA50.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli35.6% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae27.4% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis54.3% 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 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 Doravirine 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.
Sleep Outcomes and Multidimensional Assessment With Antiretroviral Therapy in People Living With HIV on Dolutegravir- vs Doravirine-Based Regimens
NCT07673965 · start 2026-08-20
Registered record
- Registry ID
- NCT07673965
- Conditions
- HIV (Human Immunodeficiency Virus); Sleep
- Interventions
- Tenofovir disoproxil fumarate 300mg / Lamivudine 300mg / Doravirine 100mg; Tenofovir disoproxil fumarate 300mg / Lamivudine 300mg / Dolutegravir 50mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Not yet recruiting
- Start
- 2026-08-20
- Completion
- 2027-11-30
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV (Human Immunodeficiency Virus); SleepInterventionTenofovir disoproxil fumarate 300mg / Lamivudine 300mg / Doravirine 100mg; Tenofovir disoproxil fumarate 300mg / Lamivudine 300mg / Dolutegravir 50mgPhasePhase 4Registry statusNot yet recruitingA Study of Doravirine/Islatravir in Healthy Lactating Females (MK-8591A-061)
NCT07086079 · start 2025-09-26
Registered record
- Registry ID
- NCT07086079
- Conditions
- Healthy
- Interventions
- DOR/ISL
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2025-09-26
- Completion
- 2026-02-04
- Enrolment
- 12
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionDOR/ISLPhasePhase 1Registry statusCompletedDOR/TDF/3TC COmpared With BIC/FTC/TAF in ART-Naïve People Living With HIV and Overweight or Obesity
NCT07075146 · start 2025-05-05
Registered record
- Registry ID
- NCT07075146
- Conditions
- HIV - Human Immunodeficiency Virus; Obesity; Overweight and/or Obesity
- Interventions
- DOR/3TC/TDF; BIC/FTC/TAF
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2025-05-05
- Completion
- 2028-08-01
- Enrolment
- 306
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV - Human Immunodeficiency Virus; Obesity; Overweight and/or ObesityInterventionDOR/3TC/TDF; BIC/FTC/TAFPhasePhase 3Registry statusRecruitingDoravirine/Lamivudine (DOR/3TC) as a Maintenance ART in Comparison With Dolutegravir/Lamivudine (DTG/3TC) in PLWH Successfully
NCT06774872 · start 2025-04-30
Registered record
- Registry ID
- NCT06774872
- Conditions
- HIV-1-infection
- Interventions
- Doravirine 100Mg Tab and Lamivudine 300 Mg Tab; Dolutegravir 50mg Tab and Lamivudine 300 Mg Tab
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2025-04-30
- Completion
- 2028-06-15
- Enrolment
- 408
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV-1-infectionInterventionDoravirine 100Mg Tab and Lamivudine 300 Mg Tab; Dolutegravir 50mg Tab and Lamivudine 300 Mg TabPhasePhase 2Registry statusRecruitingStudy Evaluating the Safety, in Terms of HBV Virological Control At 96 Weeks, of 2 Antiviral Treatment Relief Strategies, in Patients Co-infected with the HIV-1 and HBV Viruses
NCT06338826 · start 2025-02-01
Registered record
- Registry ID
- NCT06338826
- Conditions
- HIV Infections; HBV Coinfection
- Interventions
- TDF - 245mg or TAF -25mg associated to 3TC - 300mg or FTC - 200mg and a NNRTI or PI/r or INSTI; Dual therapy with 3TC in combination with DTG or ritonavir-boosted Darunavir (rDVR)
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2025-02-01
- Completion
- 2027-09-30
- Enrolment
- 140
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV Infections; HBV CoinfectionInterventionTDF - 245mg or TAF -25mg associated to 3TC - 300mg or FTC - 200mg and a NNRTI or PI/r or INSTI; Dual therapy with 3TC in combination with DTG or ritonavir-boosted Darunavir (rDVR)PhasePhase 2Registry statusNot yet recruitingA Study of Doravirine and Islatravir as a Single Entity or Combination Therapy and the Effect of Food in Healthy Adult Participants (MK-8591A-055)
NCT06719570 · start 2024-01-23
Registered record
- Registry ID
- NCT06719570
- Conditions
- Healthy
- Interventions
- MK-8591A; Islatravir; Doravine
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2024-01-23
- Completion
- 2024-03-15
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionMK-8591A; Islatravir; DoravinePhasePhase 1Registry statusCompletedThe Effect on Lipid Profile of Switching to Delstrigo in HIV Positive Patients
NCT05289986 · start 2023-11-21
Registered record
- Registry ID
- NCT05289986
- Conditions
- Hiv
- Interventions
- DELSTRIGO 100Mg-300Mg-300Mg Tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2023-11-21
- Completion
- 2024-11-21
- Enrolment
- 19
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHivInterventionDELSTRIGO 100Mg-300Mg-300Mg TabletPhasePhase 4Registry statusTerminatedB-free Multistage Trial
NCT06037564 · start 2023-11-13
Registered record
- Registry ID
- NCT06037564
- Conditions
- HIV; Drug Resistance; Drug Drug Interaction
- Interventions
- DOR/DTG/3TC
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Enrolling by invitation
- Start
- 2023-11-13
- Completion
- 2027-09
- Enrolment
- 210
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV; Drug Resistance; Drug Drug InteractionInterventionDOR/DTG/3TCPhasePhase 4Registry statusEnrolling by invitationA Randomised, Phase 3 Non-inferiority Study of DOR/3TC/TDF Compared to DTG/TAF/FTC in Participants Infected With HIV-1 Starting First-line Antiretroviral Therapy
NCT05924438 · start 2023-11-08
Registered record
- Registry ID
- NCT05924438
- Conditions
- HIV-1-infection
- Interventions
- Delstrigo; KOCITAF
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Active not recruiting
- Start
- 2023-11-08
- Completion
- 2026-06-30
- Enrolment
- 600
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV-1-infectionInterventionDelstrigo; KOCITAFPhasePhase 3Registry statusActive not recruitingDOR/ISL in HIV-1 Antiretroviral Treatment-naïve Participants (MK-8591A-053)
NCT05705349 · start 2023-03-08
Registered record
- Registry ID
- NCT05705349
- Conditions
- HIV-1 Infection
- Interventions
- DOR/ISL; BIC/FTC/TAF; Placebo to DOR/ISL; Placebo to BIC/FTC/TAF
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Active not recruiting
- Start
- 2023-03-08
- Completion
- 2029-08-05
- Enrolment
- 537
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV-1 InfectionInterventionDOR/ISL; BIC/FTC/TAF; Placebo to DOR/ISL; Placebo to BIC/FTC/TAFPhasePhase 3Registry statusActive not recruitingStudy on PhArmacokinetics of First liNe Antiretrovirals in Healthy Breastfeeding Volunteers
NCT05648201 · start 2023-03-01
Registered record
- Registry ID
- NCT05648201
- Conditions
- Hiv
- Interventions
- Doravirine 100Mg Tab; Biktarvy 50/200/25 Tab
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2023-03-01
- Completion
- 2025-04-28
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHivInterventionDoravirine 100Mg Tab; Biktarvy 50/200/25 TabPhasePhase 4Registry statusCompletedSwitch Strategy From Etravirine (ETR) to Doravirine (DOR) in Virologically-Suppressed HIV-1 Infected Adults With ETR-Resistance
NCT05506605 · start 2022-12-12
Registered record
- Registry ID
- NCT05506605
- Conditions
- HIV-1-infection
- Interventions
- Doravirine 100Mg Tab
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2022-12-12
- Completion
- 2024-12
- Enrolment
- 12
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV-1-infectionInterventionDoravirine 100Mg TabPhasePhase 4Registry statusUnknownA Cohort Study of Use of Doravirine (DOR) Based Regimens in Clinical Practice in Europe DoRavirine Europe Real World/
NCT05421806 · start 2022-10-10
Registered record
- Registry ID
- NCT05421806
- Conditions
- HIV I Infection
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Active not recruiting
- Start
- 2022-10-10
- Completion
- 2026-05
- Enrolment
- 500
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV I InfectionInterventionNot recordedPhaseNot recordedRegistry statusActive not recruitingAdipose Tissue After Switch to Doravirine
NCT05477407 · start 2022-10-06
Registered record
- Registry ID
- NCT05477407
- Conditions
- HIV Infections
- Interventions
- Switch from an INSTI-based regimen to the non INSTI-based regimen combining TDF/3TC/Doravirine
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2022-10-06
- Completion
- 2025-01-01
- Enrolment
- 22
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV InfectionsInterventionSwitch from an INSTI-based regimen to the non INSTI-based regimen combining TDF/3TC/DoravirinePhaseNot applicableRegistry statusCompletedThe Influence of Having Bariatric Surgery on the Pharmacokinetics, Safety and Efficacy of the Novel Non-nucleoside Reverse Transcriptase Inhibitor Doravirine
NCT05536466 · start 2022-09-30
Registered record
- Registry ID
- NCT05536466
- Conditions
- HIV Infections; Bariatric Surgery Candidate
- Interventions
- bariatric surgery
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2022-09-30
- Completion
- 2023-08-01
- Enrolment
- 8
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV Infections; Bariatric Surgery CandidateInterventionbariatric surgeryPhaseNot applicableRegistry statusUnknown