Study of the Efficacy and Safety of Tesevatinib in Subjects With ADPKD

PHASE2CompletedINTERVENTIONAL
Enrollment

80

Participants

Timeline

Start Date

October 12, 2017

Primary Completion Date

January 25, 2022

Study Completion Date

January 25, 2022

Conditions
Autosomal Dominant Polycystic KidneyADPKD
Interventions
DRUG

Tesevatinib

Pharmaceutical form: Tablet; Route of administration: orally

DRUG

Placebo

Pharmaceutical form: Tablet (identical to tesevatinib); Route of administration: orally

Trial Locations (19)

10016

Baylor Scott & White Research Institute, Temple

10021

Rogosin Institute, New York

19104

University of Pennsylvania, Philadelphia

21201

University of Maryland, Baltimore

22908

University of Virginia, Charlottesville

30322

Emory University School of Medicine, Atlanta

33614

Genesis Clinical Research, Tampa

33952

Coastal Nephrology Associates Research Center, LLC, Port Charlotte

53226

Medical College of Wisconsin, Milwaukee

55905

Mayo Clinic, Rochester

63110

Washington University, St Louis

80045

University of Colorado Denver, Aurora

90095

University of California Los Angeles, Los Angeles

91942

California Institute for Renal Research, La Mesa

92037

University of California San Diego, La Jolla

94143

University of California San Francisco, San Francisco

06520

Yale Nephrology Clinical Research, New Haven

02111

Tufts Medical Center, Boston

02215

Beth Israel Deaconess Medical Center, Boston

All Listed Sponsors
lead

Kadmon, a Sanofi Company

INDUSTRY

NCT03203642 - Study of the Efficacy and Safety of Tesevatinib in Subjects With ADPKD | Biotech Hunter | Biotech Hunter