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 K. pneumoniae, MRSA, 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- 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.
- Galantamine HydrobromideExisting use: Alzheimer disease, Dementia89.6% AI-predicted activityagainst K. pneumoniaeLab records exist50+ registered studies
- Chlorhexidine GluconateExisting use: Eye infection, Gingivitis, Infection and 2 more69.3% AI-predicted activityagainst K. pneumoniaeLab records exist50+ registered studies
- TriclosanExisting use: Phenol and derivatives, Medicated dressings with antiinfectives68.0% AI-predicted activityagainst K. pneumoniaeLab records exist50+ registered studies
- ElvitegravirExisting use: HIV infection, HIV-1 infection, Viral disease60.2% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Caspofungin AcetateExisting use: Aspergillosis, Candidemia, Candidiasis and 1 more57.5% AI-predicted activityagainst K. pneumoniae50+ registered studies
- DactinomycinExisting use: Kidney Wilms tumor, Neoplasm56.8% AI-predicted activityagainst K. pneumoniae50+ registered studies
- CyclosporineExisting use: Conjunctivitis, Corneal disease, Eye disease and 6 more56.1% AI-predicted activityagainst K. pneumoniae50+ registered studies
- LinaclotideExisting use: Constipation, Constipation disorder, Irritable bowel syndrome56.0% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Irinotecan HydrochlorideExisting use: Adenocarcinoma, Cancer, Carcinoma and 4 more54.5% AI-predicted activityagainst K. pneumoniae50+ registered studies
- OxytocinExisting use: Hemorrhage, Uterine Inertia52.7% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Micafungin SodiumExisting use: Candidiasis52.4% AI-predicted activityagainst K. pneumoniae50+ registered studies
- VoclosporinExisting use: Immune system disease, Lupus nephritis52.2% AI-predicted activityagainst K. pneumoniae28 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Single Arm Pilot Trial of Letermovir for CMV Prophy in CAR T Cell
NCT06575374 · start 2024-12-12
Registered record
- Registry ID
- NCT06575374
- Conditions
- Cell Therapy
- Interventions
- Letermovir
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2024-12-12
- Completion
- 2028-08-01
- Enrolment
- 36
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCell TherapyInterventionLetermovirPhasePhase 2Registry statusRecruitingClinical Trial to Evaluate the Effects of Letermovir Prophylaxis on T-cell Immune Activation in Participants With Treated HIV-1 Infection
NCT06626555 · start 2024-10
Registered record
- Registry ID
- NCT06626555
- Conditions
- HIV
- Interventions
- Letermovir
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2024-10
- Completion
- 2026-03
- Enrolment
- 36
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIVInterventionLetermovirPhasePhase 2Registry statusNot yet recruitingLetermovir (Prevymis) for CMV in Kidney and Pancreas Transplant Recipients
NCT06407232 · start 2024-08-08
Registered record
- Registry ID
- NCT06407232
- Conditions
- Cytomegalovirus Infections; Kidney Transplant Infection; Pancreas Transplant
- Interventions
- Letermovir
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2024-08-08
- Completion
- 2027-08
- Enrolment
- 90
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCytomegalovirus Infections; Kidney Transplant Infection; Pancreas TransplantInterventionLetermovirPhasePhase 3Registry statusRecruitingA Study of the Drug Letermovir as Prevention of Cytomegalovirus Infection After Stem Cell Transplant in Pediatric Patients
NCT05711667 · start 2024-07-11
Registered record
- Registry ID
- NCT05711667
- Conditions
- Hematopoietic and Lymphoid Cell Neoplasm; Malignant Solid Neoplasm
- Interventions
- Biospecimen Collection; Letermovir
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2024-07-11
- Completion
- 2029-06-30
- Enrolment
- 105
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHematopoietic and Lymphoid Cell Neoplasm; Malignant Solid NeoplasmInterventionBiospecimen Collection; LetermovirPhasePhase 3Registry statusRecruitingCMV-specific T Cell Immunity Test Indicated Prophylaxis of Letermovir After All-HSCT
NCT06449586 · start 2024-07-01
Registered record
- Registry ID
- NCT06449586
- Conditions
- Hematologic Malignancy
- Interventions
- Letermovir
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Active not recruiting
- Start
- 2024-07-01
- Completion
- 2026-06-01
- Enrolment
- 250
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHematologic MalignancyInterventionLetermovirPhasePhase 3Registry statusActive not recruitingCMV-TCIP Directed Letermovir Prophylaxis After Allo-SCT
NCT06453460 · start 2024-06-27
Registered record
- Registry ID
- NCT06453460
- Conditions
- CMV; Allogeneic Stem Cell Transplantation
- Interventions
- Letermovir; CMV T Cell Immunity Panel (CMV-TCIP); CMV DNA PCR
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2024-06-27
- Completion
- 2029-06
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCMV; Allogeneic Stem Cell TransplantationInterventionLetermovir; CMV T Cell Immunity Panel (CMV-TCIP); CMV DNA PCRPhasePhase 2Registry statusRecruitingEvaluation of the Prophylactic Use of Letermovir in Kidney Transplant Recipients at Risk of Cytomegalovirus Infection
NCT06341686 · start 2024-05-05
Registered record
- Registry ID
- NCT06341686
- Conditions
- CMV Infection
- Interventions
- Letermovir 480 MG; Ganciclovir
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Unknown
- Start
- 2024-05-05
- Completion
- 2025-05
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCMV InfectionInterventionLetermovir 480 MG; GanciclovirPhasePhase 3Registry statusUnknownEffect of Letermovir Prophylaxis on CMV-specific Immune Reconstitution Post UCBT
NCT06441669 · start 2024-05-01
Registered record
- Registry ID
- NCT06441669
- Conditions
- Cytomegalovirus Infection Reactivation
- Interventions
- Letermovir
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2024-05-01
- Completion
- 2026-05-20
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCytomegalovirus Infection ReactivationInterventionLetermovirPhaseNot recordedRegistry statusUnknownOpen Label Trial of Oral Letermovir for CMV Prophylaxis in Thoracic Transplant Recipients
NCT06066957 · start 2024-04-04
Registered record
- Registry ID
- NCT06066957
- Conditions
- Cytomegalovirus Infections; Transplant-Related Disorder
- Interventions
- Letermovir 480 MG [Prevymis]
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2024-04-04
- Completion
- 2026-08-15
- Enrolment
- 80
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCytomegalovirus Infections; Transplant-Related DisorderInterventionLetermovir 480 MG [Prevymis]PhasePhase 2Registry statusRecruitingLetermovir (LMV) Prophylaxis in CMV-seronegative Allogeneic Stem Cell Transplant Recipients With CMV Seropositive Donors: an Exploratory Study From Spanish GETH/TC Centers
NCT06211543 · start 2024-03-30
Registered record
- Registry ID
- NCT06211543
- Conditions
- CMV
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2024-03-30
- Completion
- 2026-03-30
- Enrolment
- 80
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCMVInterventionNot recordedPhaseNot recordedRegistry statusUnknownEfficacy of Letermovir in Preventing Cytomegalovirus (CMV) Infection in Lung Transplant Recipients vs. Valganciclovir.
NCT06057194 · start 2023-10
Registered record
- Registry ID
- NCT06057194
- Conditions
- Infections, Cytomegalovirus
- Interventions
- Letermovir 240 mg Oral Tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2023-10
- Completion
- 2027-04
- Enrolment
- 90
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInfections, CytomegalovirusInterventionLetermovir 240 mg Oral TabletPhasePhase 2Registry statusNot yet recruitingLetermovir for Primary Prophylaxis of Cytomegalovirus Infection After R+HID-HSCT
NCT05914675 · start 2023-07-01
Registered record
- Registry ID
- NCT05914675
- Conditions
- The Incidence of Peripheral Blood CMV Activation and Confirmed Clinically Significant CMV Infection Within 24 Weeks After Transplantation
- Interventions
- Letermovir
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2023-07-01
- Completion
- 2024-12-31
- Enrolment
- 21
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionThe Incidence of Peripheral Blood CMV Activation and Confirmed Clinically Significant CMV Infection Within 24 Weeks After TransplantationInterventionLetermovirPhasePhase 4Registry statusUnknownSecondary Prophylaxis of CMV Infection Using Letermovir After HID-HSCT
NCT05914701 · start 2023-07-01
Registered record
- Registry ID
- NCT05914701
- Conditions
- To Evaluate the Efficacy and Safety of Secondary Prophylaxis of CMV Reactivation
- Interventions
- Letermovir for secondary prophylaxis
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2023-07-01
- Completion
- 2024-12-31
- Enrolment
- 31
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTo Evaluate the Efficacy and Safety of Secondary Prophylaxis of CMV ReactivationInterventionLetermovir for secondary prophylaxisPhasePhase 4Registry statusUnknownCytomegalovirus Prophylaxis With Letermovir in Heart Transplant Recipients
NCT05432778 · start 2023-05-01
Registered record
- Registry ID
- NCT05432778
- Conditions
- CMV Viremia
- Interventions
- Letermovir Pill
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Unknown
- Start
- 2023-05-01
- Completion
- 2026-08-01
- Enrolment
- 90
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCMV ViremiaInterventionLetermovir PillPhasePhase 2Registry statusUnknownLetermovir Prophylaxis for CMV Infection in Haplo-HSCT Recipients: Single-center Data in China
NCT05789615 · start 2023-04-01
Registered record
- Registry ID
- NCT05789615
- Conditions
- CMV Infection; Hematopoietic Stem Cell Transplantation
- Interventions
- Letermovir
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2023-04-01
- Completion
- 2025-01-10
- Enrolment
- 200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCMV Infection; Hematopoietic Stem Cell TransplantationInterventionLetermovirPhaseNot recordedRegistry statusCompleted