Skip to main content

Infections, Cytomegalovirus

3
Pipeline Programs
4
Companies
2
Clinical Trials
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
1
0
2
0
0
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Vaccine
2100%
+ 2 programs with unclassified modality

Competitive Landscape

4 companies ranked by most advanced pipeline stage

MSD
MSDIreland - Ballydine
1 program
1
Letermovir 240 mg Oral TabletPhase 21 trial
Active Trials
NCT06057194Not Yet Recruiting90Est. Apr 2027
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
1 program
1
Letermovir 240 mg Oral TabletPhase 2
ViiV Healthcare
ViiV HealthcareNC - Durham
1 program
1
GSK Biologicals' Recombinant CMV gB Vaccine GSK1492903APhase 1Vaccine
GSK
GSKLONDON, United Kingdom
1 program
GSK Biologicals' Recombinant CMV gB Vaccine GSK1492903APHASE_1Vaccine1 trial
Active Trials
NCT00435396Completed40Est. Aug 2008

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
MSDLetermovir 240 mg Oral Tablet
GSKGSK Biologicals' Recombinant CMV gB Vaccine GSK1492903A

Clinical Trials (2)

Total enrollment: 130 patients across 2 trials

NCT06057194MSDLetermovir 240 mg Oral Tablet

Efficacy of Letermovir in Preventing Cytomegalovirus (CMV) Infection in Lung Transplant Recipients vs. Valganciclovir.

Start: Oct 2023Est. completion: Apr 202790 patients
Phase 2Not Yet Recruiting
NCT00435396GSKGSK Biologicals' Recombinant CMV gB Vaccine GSK1492903A

Study to Evaluate Safety and Immunogenicity of the GSK Bio CMV Vaccine in CMV-seronegative Healthy Male Adult Subjects

Start: Feb 2007Est. completion: Aug 200840 patients
Phase 1Completed

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

Vaccine is the dominant modality (100% of programs)
4 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.