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Terminated Phase 2 Interventional

Study of FibroGen (FG)-3019 in Subjects With Type 2 Diabetes Mellitus and Kidney Disease on ACEi and/or ARB Therapy

ClinicalTrials.gov ID: NCT00913393

Public ClinicalTrials.gov record NCT00913393. 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 Sep 5, 2026, 3:40 AM 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 Randomized, Double-blind, Placebo-controlled Study of FG-3019 in Subjects With Type 2 Diabetes Mellitus (DM) and Persistent Proteinuria on Background Angiotensin Converting Enzyme Inhibitor (ACEi) and/or Angiotensin II Receptor Blockade (ARB) Therapy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the effect of FG-3019 on diabetic kidney disease or diabetic nephropathy.

Study identification

NCT ID
NCT00913393
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Kyntra Bio
Industry
Enrollment
46 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 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
Jan 31, 2009
Primary completion
May 31, 2010
Completion
May 31, 2010
Last update posted
Feb 21, 2019

2009 – 2010

United States locations

U.S. sites
28
U.S. states
17
U.S. cities
28
Facility City State ZIP Site status
Not listed Tempe Arizona
Not listed Buena Park California
Not listed Lakewood California
Not listed Sacramento California
Not listed Walnut Creek California
Not listed Whittier California
Not listed Atlanta Georgia
Not listed Evergreen Park Illinois
Not listed Topeka Kansas
Not listed Wichita Kansas
Not listed Kenner Louisiana
Not listed Springfield Massachusetts
Not listed Saint Clair Shores Michigan
Not listed Lincoln Nebraska
Not listed Omaha Nebraska
Not listed Berlin New Jersey
Not listed Buffalo New York
Not listed Flushing New York
Not listed New York New York
Not listed Greenville North Carolina
Not listed Toledo Ohio
Not listed Chattanooga Tennessee
Not listed Knoxville Tennessee
Not listed Dallas Texas
Not listed Houston Texas
Not listed San Antonio Texas
Not listed Fairfax Virginia
Not listed Spokane Washington

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00913393, 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 Feb 21, 2019 · Synced Sep 5, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00913393 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →