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BK Virus Infection

2
Pipeline Programs
3
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%
+ 2 programs with unclassified modality

Competitive Landscape

3 companies ranked by most advanced pipeline stage

AiCuris
AiCurisGermany - Wuppertal
1 program
1
AIC263029Phase 21 trial
Active Trials
NCT07503561Not Yet Recruiting24Est. Dec 2026
Symbio Pharmaceuticals
1 program
1
BrincidofovirPhase 2Small Molecule1 trial
Active Trials
NCT05511779Terminated1Est. Apr 2023
Vera Therapeutics
Vera TherapeuticsBRISBANE, CA
1 program
MAU868PHASE_21 trial
Active Trials
NCT04294472Completed30Est. Feb 2022

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
AiCurisAIC263029
Symbio PharmaceuticalsBrincidofovir
Vera TherapeuticsMAU868

Clinical Trials (3)

Total enrollment: 55 patients across 3 trials

A Study to Understand How a New, Unlicensed Drug Works, Compared With a Placebo, Against BK Virus in Patients Who Have Had a Kidney Transplant.

Start: Jun 2026Est. completion: Dec 202624 patients
Phase 2Not Yet Recruiting

Study to Confirm of the Safety and Tolerability of Brincidofovir in Subjects With BK Virus Infection (Viremia) After Kidney Transplantation

Start: Oct 2022Est. completion: Apr 20231 patients
Phase 2Terminated

A Safety, Pharmacokinetics and Efficacy Study of MAU868 for the Treatment of BK Viremia in Kidney Transplant Recipients

Start: Aug 2020Est. completion: Feb 202230 patients
Phase 2Completed

Phase Legend

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

Key Insights

3 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.