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CMV

2
Pipeline Programs
5
Companies
3
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
0
0
2
0
0
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Small Molecule
1100%
+ 6 programs with unclassified modality

Competitive Landscape

5 companies ranked by most advanced pipeline stage

MSD
MSDIreland - Ballydine
2 programs
1
Letermovir PillPhase 2
Real time PCRN/A
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
2 programs
1
Letermovir PillPhase 2
Real time PCRN/A
QIAGEN
QIAGENGermany - Hilden
1 program
QuantiFERON CMV AssayN/A1 trial
Active Trials
NCT03502161Terminated8Est. Jun 2020
Merck & Co.
Merck & Co.RAHWAY, NJ
1 program
Real time PCRN/A1 trial
Active Trials
NCT04280380Unknown400Est. Dec 2022
Jazz Pharmaceuticals
Jazz PharmaceuticalsCA - Palo Alto
1 program
BrincidofovirPHASE_3Small Molecule1 trial
Active Trials
NCT01769170Completed452Est. Jan 2016

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
Jazz PharmaceuticalsBrincidofovir
Merck & Co.Real time PCR
QIAGENQuantiFERON CMV Assay

Clinical Trials (3)

Total enrollment: 860 patients across 3 trials

A Study of the Safety and Efficacy of CMX001 for the Prevention of CMV Infection in CMV-seropositive HCT Recipients

Start: Aug 2013Est. completion: Jan 2016452 patients
Phase 3Completed

Cytomegalovirus Infection in Critically Ill Patients and Patients Receiving Anticancer Therapy

Start: Mar 2020Est. completion: Dec 2022400 patients
N/AUnknown
NCT03502161QIAGENQuantiFERON CMV Assay

Clinical Evaluation of the QuantiFERON CMV Assay

Start: Nov 2018Est. completion: Jun 20208 patients
N/ATerminated

Phase Legend

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

Key Insights

5 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.