linagliptin QD (once daily) for 7 days
Drugdipeptidyl peptidase IV (DPP-4) activity will be measured as PD response to drug administration
NCT Number: NCT00935220
The objective of this trial is to investigate the pharmacokinetics and pharmacodynamics of linagliptin (BI 1356) 5 mg administered orally in patients with Type 2 diabetes mellitus of African American origin.
Looking for future studies?
Notify Me21 year–65 year
All sexes
Interventional
Phase 1
1218.55.0006 Boehringer Ingelheim Investigational Site, Cypress, California, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
dipeptidyl peptidase IV (DPP-4) activity will be measured as PD response to drug administration
Time frame: 24 hours
area under the concentration time curve (AUC_τ) of linagliptin in plasma at steady state over a uniform dosing interval
Time frame: 24 hours
maximum concentration of linagliptin in plasma at steady state
Time frame: One single measurement 24 h after drug administration under steady state conditions
Plasma DPP-4 inhibition at trough under steady state conditions. Plasma DPP-4 inhibition is derived by calculating (1-(activity in presence of linagliptin)/baseline activity))*100%, where 'activity' is the activity of the DPP-IV enzyme.
Time frame: 21 days
Frequency of patients with AEs
Time frame: 21 days
12-lead-Electrocardiogram (ECG), vital sign (blood pressure and pulse rate), physical finding and laboratory abnormalities
Time frame: 21 days
Patients with Electrocardiogram (ECG), vital signs, physical finding reported as an adverse event
Time frame: 24 hours
area under the concentration time curve of linagliptin in plasma over the time interval from 0 to 24h after administration of the first dose
Time frame: 24h
maximum concentration of linagliptin in plasma on Day 1
Time frame: One single measurement 24 h after drug administration
Plasma DPP-4 inhibition 24 hours after first dose. Plasma DPP-4 inhibition is derived by calculating (1-(activity in presence of linagliptin)/baseline activity))*100%, where 'activity' is the activity of the DPP-IV enzyme.
Boehringer Ingelheim
Industry
An Open Label, Phase I Trial to Investigate the Pharmacokinetics and Pharmacodynamics of Linagliptin (BI 1356) 5 mg After Single and Multiple Oral Administration in Patients With Type 2 Diabetes Mellitus of African American Origin for 7 Days
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT02896140
Body Weight, Diabetes Mellitus
Boston, Massachusetts, United States
View Trial DetailsNCT05035082
Diabetes Mellitus, Diabetes Mellitus, Type 2
Alhambra, California, United States
View Trial DetailsNCT06205030
Diabetes Mellitus, Diabetes Mellitus, Type 2
Kerman, Iran
View Trial DetailsNCT05370781
Diabetes Mellitus, Diabetes Mellitus, Type 2
Ann Arbor, Michigan, United States
View Trial Details