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Completed Phase 3 Interventional Results available

Safety and Efficacy of Linagliptin in Type-2-diabetes Mellitus Patients With Moderate to Severe Renal Impairment

ClinicalTrials.gov ID: NCT01087502

Public ClinicalTrials.gov record NCT01087502. 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 22, 2026, 6:34 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 Phase III, Randomised, Double-blind, Placebo-controlled Parallel Group Safety and Efficacy Study of Linagliptin (5 mg Administered Orally Once Daily) Over 12 Weeks Followed by a 40 Week Double-blind Extension Period (Placebo Patients Switched to Glimepiride) in Drug Naive or Previously Treated Type 2 Diabetic Patients With Moderate to Severe Renal Impairment and Insufficient Glycaemic Control

Study identification

NCT ID
NCT01087502
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
241 participants

Conditions and interventions

Interventions

  • Glimepiride Drug
  • Placebo Drug
  • Linagliptin 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
Feb 28, 2010
Primary completion
Apr 30, 2012
Completion
Not listed
Last update posted
Jun 26, 2014

Started 2010

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
1218.64.10007 Boehringer Ingelheim Investigational Site Chula Vista California
1218.64.10018 Boehringer Ingelheim Investigational Site Pembroke Pines Florida
1218.64.10016 Boehringer Ingelheim Investigational Site Decatur Georgia
1218.64.10015 Boehringer Ingelheim Investigational Site Boise Idaho
1218.64.10002 Boehringer Ingelheim Investigational Site Chicago Illinois
1218.64.10004 Boehringer Ingelheim Investigational Site Flint Michigan
1218.64.10006 Boehringer Ingelheim Investigational Site Kansas City Missouri
1218.64.10003 Boehringer Ingelheim Investigational Site The Bronx New York
1218.64.10013 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania
1218.64.10020 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania
1218.64.10008 Boehringer Ingelheim Investigational Site Pittsburgh Pennsylvania
1218.64.10009 Boehringer Ingelheim Investigational Site Arlington Texas
1218.64.10005 Boehringer Ingelheim Investigational Site Dallas Texas
1218.64.10011 Boehringer Ingelheim Investigational Site Houston Texas
1218.64.10014 Boehringer Ingelheim Investigational Site Houston Texas
1218.64.10010 Boehringer Ingelheim Investigational Site Tacoma Washington

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 36 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01087502, 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 26, 2014 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01087502 live on ClinicalTrials.gov.

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