Safety, Tolerability and Efficacy of AntiBKV as Treatment of BKV Infection in Kidney Transplant Recipients

PHASE2/PHASE3CompletedINTERVENTIONAL
Enrollment

95

Participants

Timeline

Start Date

April 10, 2023

Primary Completion Date

March 19, 2025

Study Completion Date

July 15, 2025

Conditions
BK Viremia; BKV DNAemia
Interventions
BIOLOGICAL

Anti-BK polyomavirus (AntiBKV)

"Participants in the study arm will each receive four doses (1,000 mg; 1,000 mg or 500 mg in the dose comparison part) of IMP administered at four-week intervals.~IMP will be administered on Days 1, 29, 57 and 85."

Trial Locations (23)

10065

New York Presbyterian Hospital - Weill Cornell Medical Center, New York

19104

University of Pennsylvania Hospital of Pennsylvania, Philadelphia

20007

MedStar Georgetown University Hospital, Washington D.C.

21201

University of Maryland, Baltimore

28207

Metrolina Nephrology Associates (MNA), PA, Charlotte

32224

Mayo Clinic Transplant Center, Jacksonville

35294

University of Alabama at Birmingham, Birmingham

43210

Ohio State University, Columbus

44195

Cleveland Clinic, Cleveland

48109

University of Michigan Health System, Ann Arbor

63110

Washington University School of Medicine in St. Louis, St Louis

66160

University of Kansas Medical Center, Kansas City

75390

UT Southwestern, Dallas

85054

Mayo Clinic, Phoenix

90024

University of California, Los Angeles, Los Angeles

90048

Cedars-Sinai Medical Center, Los Angeles

95817

University of California Davis, Sacramento

98195

University of Washington Medical Center, Seattle

06105

Hartford Hospital, Hartford

06520

Yale University School of Medicine, New Haven

02114

Massachusetts General Hospital, Boston

02215

Harvard Medical School, Boston

07039

Saint Barnabas Medical Center, Livingston

Sponsors
All Listed Sponsors
lead

Memo Therapeutics AG

INDUSTRY

NCT05769582 - Safety, Tolerability and Efficacy of AntiBKV as Treatment of BKV Infection in Kidney Transplant Recipients | Biotech Hunter | Biotech Hunter