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Completed Phase 4 Interventional Results available

Linagliptin and Metformin Versus Linagliptin in Newly Diagnosed, Untreated Type 2 Diabetes

ClinicalTrials.gov ID: NCT01512979

Public ClinicalTrials.gov record NCT01512979. 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 28, 2026, 10:53 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 24-week, Randomized, Double-blind, Active-controlled, Parallel Group Trial to Assess the Superiority of Oral Linagliptin and Metformin Compared to Linagliptin Monotherapy in Newly Diagnosed, Treatment-naïve, Uncontrolled Type 2 Diabetes Mellitus Patients

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this trial is to determine whether a initial combination of linagliptin and metformin compared to linagliptin alone for 24 weeks is effective in newly diagnosed, treatment-naïve patients with Type 2 Diabetes.

Study identification

NCT ID
NCT01512979
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
316 participants

Conditions and interventions

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
Jan 2012 (Type not available)
Primary completion
Apr 2013 (Actual)
Completion
Apr 2013 (Actual)
Last update posted
May 20, 2014

2012 – 2013

United States locations

U.S. sites
29
U.S. states
14
U.S. cities
29
Facility City State ZIP Site status
1218.83.11002 Boehringer Ingelheim Investigational Site Phoenix Arizona — —
1218.83.11036 Boehringer Ingelheim Investigational Site Little Rock Arkansas — —
1218.83.11011 Boehringer Ingelheim Investigational Site Chino California — —
1218.83.11001 Boehringer Ingelheim Investigational Site Huntington Beach California — —
1218.83.11019 Boehringer Ingelheim Investigational Site Huntington Park California — —
1218.83.11015 Boehringer Ingelheim Investigational Site Lomita California — —
1218.83.11023 Boehringer Ingelheim Investigational Site Norwalk California — —
1218.83.11014 Boehringer Ingelheim Investigational Site Roseville California — —
1218.83.11031 Boehringer Ingelheim Investigational Site San Diego California — —
1218.83.11022 Boehringer Ingelheim Investigational Site Fort Lauderdale Florida — —
1218.83.11025 Boehringer Ingelheim Investigational Site Orlando Florida — —
1218.83.11033 Boehringer Ingelheim Investigational Site Sanford Florida — —
1218.83.11029 Boehringer Ingelheim Investigational Site Oakwood Georgia — —
1218.83.11026 Boehringer Ingelheim Investigational Site Owensboro Kentucky — —
1218.83.11008 Boehringer Ingelheim Investigational Site Elkton Maryland — —
1218.83.11027 Boehringer Ingelheim Investigational Site Freemont Nebraska — —
1218.83.11005 Boehringer Ingelheim Investigational Site Edison New Jersey — —
1218.83.11013 Boehringer Ingelheim Investigational Site Jacksonville North Carolina — —
1218.83.11028 Boehringer Ingelheim Investigational Site Salisbury North Carolina — —
1218.83.11009 Boehringer Ingelheim Investigational Site Shelby North Carolina — —
1218.83.11003 Boehringer Ingelheim Investigational Site Franklin Ohio — —
1218.83.11024 Boehringer Ingelheim Investigational Site Gallipolis Ohio — —
1218.83.11018 Boehringer Ingelheim Investigational Site Columbia South Carolina — —
1218.83.11004 Boehringer Ingelheim Investigational Site Bristol Tennessee — —
1218.83.11017 Boehringer Ingelheim Investigational Site Chattanooga Tennessee — —
1218.83.11032 Boehringer Ingelheim Investigational Site Grand Prairie Texas — —
1218.83.11030 Boehringer Ingelheim Investigational Site Houston Texas — —
1218.83.11034 Boehringer Ingelheim Investigational Site San Antonio Texas — —
1218.83.11021 Boehringer Ingelheim Investigational Site Tomball Texas — —

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 53 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01512979, 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 May 20, 2014 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01512979 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →