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Completed Phase 2 Interventional Results available

Safety and Efficacy of Different Oral Doses of BAY94-8862 in Subjects With Type 2 Diabetes Mellitus and the Clinical Diagnosis of Diabetic Nephropathy

ClinicalTrials.gov ID: NCT01874431

Public ClinicalTrials.gov record NCT01874431. 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, 12:29 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 Randomized, Double-blind, Placebo-controlled, Multi-center Study to Assess the Safety and Efficacy of Different Oral Doses of BAY94-8862 in Subjects With Type 2 Diabetes Mellitus and the Clinical Diagnosis of Diabetic Nephropathy

Study identification

NCT ID
NCT01874431
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bayer
Industry
Enrollment
823 participants

Conditions and interventions

Interventions

  • Finerenone (BAY94-8862) Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Jun 11, 2013
Primary completion
Jul 8, 2014
Completion
Aug 6, 2014
Last update posted
Jun 30, 2021

2013 – 2014

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Not listed Birmingham Alabama 35294
Not listed Chula Vista California 91910
Not listed Los Angeles California 90022
Not listed Los Gatos California 95032
Not listed New Haven Connecticut 06510
Not listed Miami Florida 33015
Not listed Pembroke Pines Florida 33028
Not listed Chicago Illinois 60611
Not listed Chicago Illinois 60612
Not listed Flint Michigan 48504
Not listed Flushing New York 11355
Not listed Orangeburg South Carolina 29118
Not listed Chattanooga Tennessee 37408
Not listed Dallas Texas 75235-3858
Not listed Burlington Vermont 05401

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 132 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01874431, 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 Jun 30, 2021 · Synced Jul 23, 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 NCT01874431 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →