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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 Oct 20, 2026, 5:15 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
Feb 2009 (Type not available)
Primary completion
Jun 2010 (Actual)
Completion
Jun 2010 (Actual)
Last update posted
Feb 22, 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 22, 2019 · Synced Oct 20, 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 public registry record, listed eligibility criteria, and available contact information for NCT00913393 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →