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NCT01874431 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by Bayer.

Completed
Registry status
Phase 2
Development phase
823
Enrollment target

NCT01874431: Completed Phase 2 study, sponsored by Bayer.

NCT01874431 is a Phase 2 study that has completed, run by Bayer. The registered enrollment target is 823 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (519% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01874431, a Phase 2 study, has completed, sponsored by Bayer.

COMPLETED
Registry status
Phase 2
Development phase
823 participants
Enrollment target

Study Summary

To assess a new drug, BAY94-8862 given orally at different doses, to evaluate whether it was safe and can help the well being of patients with type 2 diabetes and diabetic nephropathy. These treatment doses were compared to placebo.

Primary Outcome

Albumin-to-creatinine ratio (UACR) is defined as gram of albumin per kilogram of creatinine. UACR was calculating the average of 3 first morning void samples taken on 3 consecutive days.

Interventions

  • DRUG Placebo
  • DRUG Finerenone (BAY94-8862)

Trial Details

FieldValue
Enrollment Target 823 participants
Start Date 2013-06-12
Est. Completion 2014-08-07
Phase Phase 2
Bayer

591 total trials

What the finished NCT01874431 record still lists

NCT01874431 is an interventional study that assigns participants to a tested intervention. The registered 823 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (519% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT01874431 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01874431 about?

NCT01874431 is a clinical study titled "Safety and Efficacy of Different Oral Doses of BAY94-8862 in Subjects With Type 2 Diabetes Mellitus and the Clinical Diagnosis of Diabetic Nephropathy". To assess a new drug, BAY94-8862 given orally at different doses, to evaluate whether it was safe and can help the well being of patients with type 2 diabetes and diabetic nephropathy. These treatment doses were compared to placebo.

What is the current status of trial NCT01874431?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 823 participants. The study started on 2013-06-12. Estimated completion is 2014-08-07.

What interventions are being tested in trial NCT01874431?

The interventions under investigation include: Placebo (DRUG), Finerenone (BAY94-8862) (DRUG).

Who is sponsoring clinical trial NCT01874431?

This trial is sponsored by Bayer, which has 591 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01874431's enrollment target sits among peer trials

823 36th of 2000 higher than 1,965 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01874431, the US trial registry maintained by the National Library of Medicine. NCT01874431 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.