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Completed Phase 2 Interventional Results available

Bosutinib For Autosomal Dominant Polycystic Kidney Disease

ClinicalTrials.gov ID: NCT01233869

Public ClinicalTrials.gov record NCT01233869. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 8:34 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study Of The Safety, Clinical Activity And Pharmacokinetics Of Bosutinib (PF-05208763) Versus Placebo In Subjects With Autosomal Dominant Polycystic Kidney Disease (ADPKD)

Study identification

NCT ID
NCT01233869
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
172 participants

Conditions and interventions

Interventions

  • Bosutinib Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 50 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2010
Primary completion
Jun 30, 2014
Completion
Jul 31, 2014
Last update posted
Mar 10, 2016

2010 – 2014

United States locations

U.S. sites
20
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Southwest Kidney Institute, PLC Phoenix Arizona 85004
Southwest Clinical Research Institute, LLC Tempe Arizona 85284
Southwest Kidney Institute, PLC Tempe Arizona 85284
Capital Nephrology Clinical Research Sacramento California 95825
Boise Kidney & Hypertension Institute, PLLC Caldwell Idaho 83605
Boise Kidney & Hypertension Institute, PLLC Meridian Idaho 83642
Renal Associates of Baton Rouge Baton Rouge Louisiana 70808
Tufts Medical Center Boston Massachusetts 02111
Washington University School of Medicine St Louis Missouri 63110
Washington University St Louis Missouri 63110
New York University - HHC CTSI Clinical Research Center New York New York 10016
Doylestown Hospital MRI Doylestown Pennsylvania 18901
Doylestown Hospital Doylestown Pennsylvania 18901
Nephrology/Hypertension Specialists Doylestown Pennsylvania 18901
Renal Associates, PA San Antonio Texas 78215
San Antonio Kidney Disease Center Physicians Group, P.L.L.C. San Antonio Texas 78229
University of Virginia Health System - Nephrology Charlottesville Virginia 22908
University of Virginia Health System Charlottesville Virginia 22908
The Polyclinic Seattle Washington 98104
Renal Remission and Hypertension Clinic Silverdale Washington 98383

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 47 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01233869, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 10, 2016 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01233869 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →