A Study on Spermatogenesis in Male Renal Transplant Recipients Receiving Valganciclovir (Valcyte®) Versus Untreated Matched Controls

PHASE4CompletedINTERVENTIONAL
Enrollment

59

Participants

Timeline

Start Date

January 30, 2012

Primary Completion Date

September 29, 2015

Study Completion Date

December 30, 2016

Conditions
Cytomegalovirus Infections
Interventions
DRUG

Valganciclovir

Participants will receive valganciclovir 900 milligrams (mg) orally once daily for up to a maximum of 200 days post-transplant.

Trial Locations (19)

11794

Stony Brook University Hospital, Stony Brook

12208

Albany Medical Cancer Center, Albany

14203

University at Buffalo, Buffalo

19102

Drexel University Department of Nephrology, Philadelphia

20010

Washington Hospital Center, Washington D.C.

20230

Hospital Miguel Hidalgo, Aguascalientes

30912

Medical College of Georgia, Augusta

55455

University of Minnesota, Minneapolis

55902

Mayo Clinic Rochester, Rochester

62448

Instituto Mexicano de Trasplantes, Cuernavaca

78229

Methodist Healthcare System of San Antonio, San Antonio

78240

Hospital Central Dr. Ignacio Morones Prieto, San Luis Potosí City

90057

National Institute of Transplantation, Los Angeles

90095

University of California Los Angeles (UCLA), Los Angeles

94115

University of California at San Francisco, San Francisco

97237

Oregan Health & Science Univ, Portland

02111

Tufts Medical Center, Boston

01107

Western New England Renal & Transplant Associates, P.C., Springfield

02903

Rhode Island Hospital, Providence

All Listed Sponsors
lead

Hoffmann-La Roche

INDUSTRY

NCT01663740 - A Study on Spermatogenesis in Male Renal Transplant Recipients Receiving Valganciclovir (Valcyte®) Versus Untreated Matched Controls | Biotech Hunter | Biotech Hunter