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

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTI-CENTER STUDY TO ASSESS THE SAFETY AND EFFICACY OF DIFFERENT ORAL DOSES OF BAY 94-8862 IN SUBJECTS WITH TYPE 2 DIABETES MELLITUS AND THE CLINICAL DIAGNOSIS OF DIABETIC NEPHROPATHY.

Intervention/treatment:
FINERENONE (BAY 94-8862)
Medical condition:
DIABETIC NEUROPATHIC PAIN
Protocol code:
16243
Control number:
164793
Status:
Closed
Approved:
June 07, 2013
Date Completed:
Trial phase:
Phase 2
For more information:
ClinicalTrials.gov - NCT01874431
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Therapeutic Area Head
Organization
Bayer AG
Sponsor
BAYER INC

Locations

British Columbia

Vancouver, British Columbia, V5Z 1L8
Vancouver, British Columbia, V6E 1M7

Ontario

Courtice, Ontario, L1E 3C3
Kitchener, Ontario, N2H 5Z8
Scarborough Village, Ontario, M1H 3G4
Toronto, Ontario, M4C 5T2
Toronto, Ontario, M4N 3M5

Quebec

Montreal, Quebec, H1T 2M4

Results

See the results from the trial NCT01874431. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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