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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01087502
Other study ID # 1218.64
Secondary ID 2009-016971-31
Status Completed
Phase Phase 3
First received March 15, 2010
Last updated June 17, 2014
Start date March 2010

Study information

Verified date May 2014
Source Boehringer Ingelheim
Contact n/a
Is FDA regulated No
Health authority Australia: Dept of Health and Ageing Therapeutic Goods AdminCanada: Health CanadaFinland: Finnish Medicines AgencyIsrael: Israeli Health Ministry Pharmaceutical AdministrationJapan: Ministry of Health, Labor and WelfareNew Zealand: Multi-Regional Ethics CommitteeSlovakia: State Institute for Drug ControlSweden: Medical Products AgencyUnited States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The objective of the current study is to investigate the efficacy, safety and tolerability of linagliptin (5 mg / once daily) compared to placebo given over 12 weeks in drug naive or previously treated type 2 diabetic patients with moderate to severe renal impairment and insufficient glycaemic control. In addition safety in this patient population with longer term (40 week) treatment in comparison to sulfonylurea drug (glimepiride).


Recruitment information / eligibility

Status Completed
Enrollment 241
Est. completion date
Est. primary completion date May 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion criteria:

1. Type 2 diabetes mellitus

2. GFR<60 ml/min

3. HbA1c >=7.0% to <= 10%

4. Age >= 18 years

5. BMI <=45 kg/m2

6. Signed and dated written informed consent

Exclusion criteria:

1. Myocardial infarction, stroke or TIA within 3 months prior to informed consent

2. Renal impairment requiring dialysis

3. Bariatric surgery

4. Impaired hepatic function

5. Treatment with glitazones, GLP-1 analogues, DPP-4 inhibitors

6. Treatment with anti-obesity drugs

7. Treatment with SU, glinides and metformin 8 weeks prior to informed consent

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Intervention

Drug:
Glimepiride
1-4 mg daily after 12 weeks
Placebo
Placebo mach to 5 mg linagliptin first 12 weeks of treatment once daily
Placebo
Placebo maching Glimepiride 1-4 mg after 12 weeks of treatment
Placebo
Placebo mach to 5 mg linagliptin once daily after 12 weeks
Linagliptin
5 mg once daily

Locations

Country Name City State
Australia 1218.64.61003 Boehringer Ingelheim Investigational Site Adelaide South Australia
Australia 1218.64.61005 Boehringer Ingelheim Investigational Site Gosford New South Wales
Australia 1218.64.61001 Boehringer Ingelheim Investigational Site Liverpool New South Wales
Australia 1218.64.61004 Boehringer Ingelheim Investigational Site Reservoir Victoria
Australia 1218.64.61002 Boehringer Ingelheim Investigational Site St Leonards New South Wales
Canada 1218.64.20008 Boehringer Ingelheim Investigational Site Corunna Ontario
Canada 1218.64.20005 Boehringer Ingelheim Investigational Site Hamilton Ontario
Canada 1218.64.20007 Boehringer Ingelheim Investigational Site Hamilton Ontario
Canada 1218.64.20003 Boehringer Ingelheim Investigational Site Point Claire Quebec
Canada 1218.64.20002 Boehringer Ingelheim Investigational Site Sarnia Ontario
Canada 1218.64.20009 Boehringer Ingelheim Investigational Site Stayner Ontario
Canada 1218.64.20004 Boehringer Ingelheim Investigational Site Toronto Ontario
Finland 1218.64.35804 Boehringer Ingelheim Investigational Site Kokkola
Finland 1218.64.35803 Boehringer Ingelheim Investigational Site Oulu
Finland 1218.64.35801 Boehringer Ingelheim Investigational Site Turku
Israel 1218.64.97204 Boehringer Ingelheim Investigational Site Ashkelon
Israel 1218.64.97207 Boehringer Ingelheim Investigational Site Givatayim
Israel 1218.64.97203 Boehringer Ingelheim Investigational Site Haifa
Israel 1218.64.97201 Boehringer Ingelheim Investigational Site Jerusalem
Israel 1218.64.97202 Boehringer Ingelheim Investigational Site Nahariya
Israel 1218.64.97206 Boehringer Ingelheim Investigational Site Tel Aviv
Japan 1218.64.81005 Boehringer Ingelheim Investigational Site Asahi, Chiba
Japan 1218.64.81006 Boehringer Ingelheim Investigational Site Isesaki, Gunma
Japan 1218.64.81001 Boehringer Ingelheim Investigational Site Meguro-ku, Tokyo
Japan 1218.64.81008 Boehringer Ingelheim Investigational Site Nagoya, Aichi
Japan 1218.64.81007 Boehringer Ingelheim Investigational Site Osaka, Osaka
Japan 1218.64.81002 Boehringer Ingelheim Investigational Site Shinjyuku-ku,Tokyo
Japan 1218.64.81004 Boehringer Ingelheim Investigational Site Suita, Osaka
Japan 1218.64.81003 Boehringer Ingelheim Investigational Site Suwa, Nagano
New Zealand 1218.64.64001 Boehringer Ingelheim Investigational Site Otahuhu Auckland
Slovakia 1218.64.42102 Boehringer Ingelheim Investigational Site Bratislava
Slovakia 1218.64.42107 Boehringer Ingelheim Investigational Site Kosice
Slovakia 1218.64.42109 Boehringer Ingelheim Investigational Site Nitra
Slovakia 1218.64.42108 Boehringer Ingelheim Investigational Site Trencin
Sweden 1218.64.46002 Boehringer Ingelheim Investigational Site Härnösand
Sweden 1218.64.46003 Boehringer Ingelheim Investigational Site Helsingborg
United States 1218.64.10009 Boehringer Ingelheim Investigational Site Arlington Texas
United States 1218.64.10015 Boehringer Ingelheim Investigational Site Boise Idaho
United States 1218.64.10003 Boehringer Ingelheim Investigational Site Bronx New York
United States 1218.64.10002 Boehringer Ingelheim Investigational Site Chicago Illinois
United States 1218.64.10007 Boehringer Ingelheim Investigational Site Chula Vista California
United States 1218.64.10005 Boehringer Ingelheim Investigational Site Dallas Texas
United States 1218.64.10016 Boehringer Ingelheim Investigational Site Decatur Georgia
United States 1218.64.10004 Boehringer Ingelheim Investigational Site Flint Michigan
United States 1218.64.10011 Boehringer Ingelheim Investigational Site Houston Texas
United States 1218.64.10014 Boehringer Ingelheim Investigational Site Houston Texas
United States 1218.64.10006 Boehringer Ingelheim Investigational Site Kansas City Missouri
United States 1218.64.10018 Boehringer Ingelheim Investigational Site Pembroke Pines Florida
United States 1218.64.10013 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania
United States 1218.64.10020 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania
United States 1218.64.10008 Boehringer Ingelheim Investigational Site Pittsburgh Pennsylvania
United States 1218.64.10010 Boehringer Ingelheim Investigational Site Tacoma Washington

Sponsors (2)

Lead Sponsor Collaborator
Boehringer Ingelheim Eli Lilly and Company

Countries where clinical trial is conducted

United States,  Australia,  Canada,  Finland,  Israel,  Japan,  New Zealand,  Slovakia,  Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary HbA1c Change From Baseline to Week 12 HbA1c is measured as a percentage. Thus, this change from baseline reflects the Week 12 HbA1c percent minus the baseline HbA1c percent. Means are treatment adjusted for baseline HbA1c, renal function impairment and prior use of antidiabetic agents. Baseline and week 12 No
Secondary HbA1c Change From Baseline Over Time HbA1c is measured as a percentage. Thus, this change from baseline reflects the HbA1c percent over time minus the baseline HbA1c percent. This outcome measure only provides descriptive statistics without any modelling. Baseline, week 4, week 8, week 12, week 16, week 20, week 24, week 28, week 34, week 40, week 46, week 52 No
Secondary Fasting Plasma Glucose (FPG) Change From Baseline to Week 12 This change from baseline reflects the Week 12 FPG minus the baseline FPG. Means are treatment-adjusted for baseline HbA1c, baseline FPG and prior use of insulin, week repeated within patient and week by treatment interaction. Baseline and week 12 No
Secondary Fasting Plasma Glucose (FPG) Change From Baseline Over Time This change from baseline reflects the FPG over time minus the baseline FPG. This outcome measure only provides descriptive statistics without any modelling. Baseline, week 4, week 8, week 12, week 20, week 24, week 28, week 34, week 40, week 46, week 52 No
Secondary Percentage of Patients With HbA1c <7.0% The percentage of patients with an HbA1c value below 7% at week 12 and week 52 were calculated for each treatment arm. If a patient did not have an HbA1c value at week 12 or 52 respectively, they were considered a failure, so HbA1c above 7%. Baseline, week 12 and week 52 No
Secondary Percentage of Patients With HbA1c <6.5% The percentage of patients with an HbA1c value below 6.5% at week 12 and week 52 was calculated for each treatment arm. If a patient did not have an HbA1c value at week 12 or 52 respectively they were considered a failure, so HbA1c above 6.5%. Baseline, week 12 and week 52 No
Secondary Percentage of Patients Who Have a HbA1c Lowering by at Least 0.5% The percentage of patients with an HbA1c reduction of =0.5% at week 12 and week 52 from baseline was calculated for each treatment arm. If a patient did not have an HbA1c value at week 12 or 52 respectively they were considered a failure, so HbA1c reduction less than 0.5%. Baseline, week 12 and week 52 No
Secondary Plasma Concentration of Linagliptin at Trough Trough levels of concentration of Linagliptin in plasma. Week 12, 24 and 52 No
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