Efficacy and Safety of BI 1356 (Linagliptin) Versus Placebo in Type 2 Diabetic Patients With Insufficient Glycemic Control

NCT00621140 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 503

Last updated 2014-02-17

Study results available
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Summary

To investigate efficacy, safety and tolerability of BI 1356 versus placebo

Conditions

  • Diabetes Mellitus, Type 2

Interventions

DRUG

linagliptin

active

DRUG

placebo

placebo

Sponsors & Collaborators

Principal Investigators

  • Boehringer Ingelheim · Boehringer Ingelheim

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-02-29
Primary Completion
2009-05-31

Countries

  • Croatia
  • India
  • Israel
  • Italy
  • Malaysia
  • Netherlands
  • Poland
  • Romania
  • Slovakia
  • Thailand
  • Ukraine

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00621140 on ClinicalTrials.gov