Letermovir
FDA-approved product (tablet, oral), marketed as Prevymis.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 4 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Cytomegalovirus infection
- Infection
- Viral disease
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Other antivirals
- FDA pharmacologic class
- Cytomegalovirus DNA Terminase Complex Inhibitor FDA label ↗
- Anti-infective classification
- Classified as another kind of anti-infective (for example an antifungal, antiviral or antiparasitic medicine).WHO ATC J05AX18
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against M. tuberculosis, MRSA, E. coli and K. pneumoniae. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA58.6% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli46.2% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae49.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- M. tuberculosis64.9% 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
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 Letermovir 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.
- Pitavastatin SodiumExisting use: Abnormal circulating lipid concentration, Cardiovascular disease, Familial hypercholesterolemia and 2 more66.8% AI-predicted activityagainst M. tuberculosis18 registered studies
- AmisulprideExisting use: Nausea and vomiting, Post operative nausea and vomiting, Psychosis66.8% AI-predicted activityagainst M. tuberculosis50+ registered studies
- ItraconazoleExisting use: Aspergillosis, Blastomycosis, Candidiasis and 4 more66.7% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Dantrolene SodiumExisting use: Cerebral palsy, Fever, Malignant hyperthermia and 4 more66.6% AI-predicted activityagainst M. tuberculosis12 registered studies
- LurbinectedinExisting use: Cancer, Neoplasm, Small cell lung carcinoma66.6% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Methixene HydrochlorideExisting use: Parkinson disease66.6% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- Cisapride MonohydrateExisting use: Gastrointestinal disease66.5% AI-predicted activityagainst M. tuberculosis5 registered studies
- Angiotensin Ii AcetateExisting use: Cardiovascular disease, Hypotension, Septic shock and 1 more66.3% AI-predicted activityagainst M. tuberculosis10 registered studies
- QuazepamExisting use: Insomnia66.3% AI-predicted activityagainst M. tuberculosis1 registered study
- AbemaciclibExisting use: Breast cancer, Breast carcinoma, Breast neoplasm and 3 more66.2% AI-predicted activityagainst M. tuberculosis50+ registered studies
- TerconazoleExisting use: Triazole derivatives66.2% AI-predicted activityagainst M. tuberculosis10 registered studies
- Degarelix AcetateExisting use: Prostate adenocarcinoma, Prostate cancer, Prostate carcinoma66.0% AI-predicted activityagainst M. tuberculosis50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
A Study of Letermovir (MK-8228) to Evaluate Efficacy and Safety for Prevention of Cytomegalovirus Infection in Chinese Hematopoietic Stem Cell Transplant Recipients (MK-8228-045)
NCT05763823 · start 2023-03-24
Registered record
- Registry ID
- NCT05763823
- Conditions
- Cytomegalovirus Infection
- Interventions
- Letermovir
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2023-03-24
- Completion
- 2024-04-18
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCytomegalovirus InfectionInterventionLetermovirPhasePhase 3Registry statusCompletedLetermovir for Secondary Prophylaxis in Solid Organ Transplant Recipients
NCT05626530 · start 2023-02-02
Registered record
- Registry ID
- NCT05626530
- Conditions
- Cytomegalovirus Infections; Infection in Solid Organ Transplant Recipients; Neutropenia; Antiviral Toxicity
- Interventions
- Letermovir
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2023-02-02
- Completion
- 2025-12-15
- Enrolment
- 25
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCytomegalovirus Infections; Infection in Solid Organ Transplant Recipients; Neutropenia; Antiviral ToxicityInterventionLetermovirPhasePhase 4Registry statusRecruitingHCMV Breakthrough Infections During Letermovir Prophylaxis
NCT06339892 · start 2023-01-09
Registered record
- Registry ID
- NCT06339892
- Conditions
- Cytomegalovirus Infections; Cytomegalovirus Viremia; Hematopoietic Stem Cell Transplantation
- Interventions
- Determination of HCMV DNA in plasma after DNAse digestion.; Determination of HCMV DNA in blood or plasma.
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2023-01-09
- Completion
- 2026-03
- Enrolment
- 140
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCytomegalovirus Infections; Cytomegalovirus Viremia; Hematopoietic Stem Cell TransplantationInterventionDetermination of HCMV DNA in plasma after DNAse digestion.; Determination of HCMV DNA in blood or plasma.PhaseNot applicableRegistry statusUnknownImmune Reconstitution to CMV After HSCT: Impact of Clinical Factors and Therapy Strategies
NCT05656599 · start 2023-01-03
Registered record
- Registry ID
- NCT05656599
- Conditions
- CMV Infection; Hematopoietic Stem Cell Transplantation
- Interventions
- Letermovir
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2023-01-03
- Completion
- 2025-12
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCMV Infection; Hematopoietic Stem Cell TransplantationInterventionLetermovirPhaseNot recordedRegistry statusUnknownObservational Clinical Study of Letermovir for Preventing CMV Infection After Allo-HSCT
NCT06306989 · start 2023-01-01
Registered record
- Registry ID
- NCT06306989
- Conditions
- Letemovir for the Prevention of CMV Infection After Allo-HSCT
- Interventions
- Letermovir
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2023-01-01
- Completion
- 2025-12-01
- Enrolment
- 150
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLetemovir for the Prevention of CMV Infection After Allo-HSCTInterventionLetermovirPhaseNot recordedRegistry statusUnknownLetermovir in ART-treated HIV-infected Persons
NCT05362916 · start 2022-09-26
Registered record
- Registry ID
- NCT05362916
- Conditions
- People Living With HIV
- Interventions
- Letermovir
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2022-09-26
- Completion
- 2025-01-27
- Enrolment
- 33
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPeople Living With HIVInterventionLetermovirPhaseNot applicableRegistry statusCompletedA Study to Evaluate the Anti-inflammatory Effects of Letermovir (Prevymis) in Adults With Human Immunodeficiency Virus (HIV)-1 and Asymptomatic Cytomegalovirus (CMV) Who Are on Suppressive Antiretroviral Therapy, Plus Its Effect on Chronic Inflammation, HIV Persistence and Other Clinical Outcomes.
NCT04840199 · start 2022-04-19
Registered record
- Registry ID
- NCT04840199
- Conditions
- HIV Infections; Cytomegalovirus; CMV
- Interventions
- Letermovir Oral Tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2022-04-19
- Completion
- 2023-11-30
- Enrolment
- 44
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV Infections; Cytomegalovirus; CMVInterventionLetermovir Oral TabletPhasePhase 2Registry statusTerminatedLetermovir Use in Heart Transplant Recipients
NCT04904614 · start 2022-01-05
Registered record
- Registry ID
- NCT04904614
- Conditions
- Cytomegalovirus Disease; Cytomegalovirus Infections; Heart Transplant Infection; Antiviral Toxicity; Neutropenia
- Interventions
- Letermovir
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2022-01-05
- Completion
- 2025-01-14
- Enrolment
- 32
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCytomegalovirus Disease; Cytomegalovirus Infections; Heart Transplant Infection; Antiviral Toxicity +1 moreInterventionLetermovirPhasePhase 4Registry statusCompletedLetermovir for CMV Prevention After Lung Transplantation
NCT05041426 · start 2021-12-06
Registered record
- Registry ID
- NCT05041426
- Conditions
- Lung Transplant; CMV
- Interventions
- Letermovir; Valganciclovir
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2021-12-06
- Completion
- 2025-03-03
- Enrolment
- 15
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLung Transplant; CMVInterventionLetermovir; ValganciclovirPhasePhase 2Registry statusCompletedPrenatal Treatment of Congenital Cytomegalovirus Infection With Letermovir Randomized Against Valaciclovir - CYMEVALIII STEP1
NCT04732260 · start 2021-06-11
Registered record
- Registry ID
- NCT04732260
- Conditions
- Pregnant Women Undergoing TOP; TOP - Failed Attempted Termination of Pregnancy
- Interventions
- Letermovir
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2021-06-11
- Completion
- 2021-11-12
- Enrolment
- 7
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPregnant Women Undergoing TOP; TOP - Failed Attempted Termination of PregnancyInterventionLetermovirPhaseNot applicableRegistry statusCompletedLetermovir for the Prevention of Cytomegalovirus Reactivation in Patients With Hematological Malignancies Treated With Alemtuzumab
NCT04312841 · start 2020-09-15
Registered record
- Registry ID
- NCT04312841
- Conditions
- B-Cell Prolymphocytic Leukemia; Chronic Lymphocytic Leukemia; Peripheral T-Cell Lymphoma; Primary Cutaneous T-Cell Non-Hodgkin Lymphoma; Sezary Syndrome; T-Cell Prolymphocytic Leukemia
- Interventions
- Letermovir
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2020-09-15
- Completion
- 2024-04-09
- Enrolment
- 6
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionB-Cell Prolymphocytic Leukemia; Chronic Lymphocytic Leukemia; Peripheral T-Cell Lymphoma; Primary Cutaneous T-Cell Non-Hodgkin Lymphoma +2 moreInterventionLetermovirPhasePhase 2Registry statusCompletedMK-8228 (Letermovir) in the Prevention of Human Cytomegalovirus (CMV) Infection and Disease in Adult Japanese Kidney Transplant Recipients (MK-8228-042)
NCT04129398 · start 2019-12-27
Registered record
- Registry ID
- NCT04129398
- Conditions
- Cytomegalovirus Infection; Cytomegalovirus Disease
- Interventions
- Letermovir tablet; Letermovir IV
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2019-12-27
- Completion
- 2022-10-06
- Enrolment
- 22
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCytomegalovirus Infection; Cytomegalovirus DiseaseInterventionLetermovir tablet; Letermovir IVPhasePhase 3Registry statusCompletedTriplex Vaccine in Preventing CMV Infection in Patients Undergoing Hematopoietic Stem Cell Transplantation
NCT04060277 · start 2019-11-27
Registered record
- Registry ID
- NCT04060277
- Conditions
- Accelerated Phase Chronic Myelogenous Leukemia, BCR-ABL1 Positive; Acute Lymphoblastic Leukemia; Acute Myeloid Leukemia; Chronic Lymphocytic Leukemia; Chronic Phase Chronic Myelogenous Leukemia, BCR-ABL1 Positive; Hematopoietic and Lymphoid Cell Neoplasm; Hodgkin Lymphoma; Lymphoblastic Lymphoma; Myelodysplastic Syndrome; Myelofibrosis; Myeloproliferative Neoplasm; Non-Hodgkin Lymphoma
- Interventions
- Letermovir; Multi-peptide CMV-Modified Vaccinia Ankara Vaccine; Placebo Administration
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Active not recruiting
- Start
- 2019-11-27
- Completion
- 2030-04-07
- Enrolment
- 7
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAccelerated Phase Chronic Myelogenous Leukemia, BCR-ABL1 Positive; Acute Lymphoblastic Leukemia; Acute Myeloid Leukemia; Chronic Lymphocytic Leukemia +8 moreInterventionLetermovir; Multi-peptide CMV-Modified Vaccinia Ankara Vaccine; Placebo AdministrationPhasePhase 2Registry statusActive not recruitingLetermovir Treatment in Pediatric Participants Following Allogeneic Haematopoietic Stem Cell Transplantation (HSCT) (MK-8228-030)
NCT03940586 · start 2019-08-08
Registered record
- Registry ID
- NCT03940586
- Conditions
- Cytomegalovirus (CMV) Infection
- Interventions
- Letermovir oral granules; Letermovir tablet; Letermovir intravenous
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2019-08-08
- Completion
- 2023-08-25
- Enrolment
- 65
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCytomegalovirus (CMV) InfectionInterventionLetermovir oral granules; Letermovir tablet; Letermovir intravenousPhasePhase 2Registry statusCompletedA Study of the Drug Letermovir (LTV) as Prevention for Recurrent of Cytomegalovirus (CMV) Infection
NCT04017962 · start 2019-07-19
Registered record
- Registry ID
- NCT04017962
- Conditions
- CMV; CMV Infection; Hematopoietic Cell Transplant
- Interventions
- Letermovir Pill; blood draw
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2019-07-19
- Completion
- 2025-07-29
- Enrolment
- 102
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCMV; CMV Infection; Hematopoietic Cell TransplantInterventionLetermovir Pill; blood drawPhasePhase 2Registry statusCompleted