| Trial ID: | L3598 |
| Source ID: | NCT01436201
|
| Associated Drug: |
Digoxin
|
| Title: |
A Study of the Effect of Dulaglutide on How Body Handles Digoxin in Healthy Participants
|
| Acronym: |
|
| Status: |
COMPLETED
|
| Study Results: |
YES
|
| Results: |
https://ClinicalTrials.gov/show/NCT01436201/results
|
| Conditions: |
Diabetes Mellitus, Type 2
|
| Interventions: |
DRUG: Digoxin|BIOLOGICAL: Dulaglutide
|
| Outcome Measures: |
Primary: Pharmacokinetics: Area Under the Concentration Versus Time Curve (AUC) of Digoxin, Predose (Digoxin) and up to 24 hours postdose on Days 7, 10, and 17|Pharmacokinetics: Maximum Observed Drug Concentration (Cmax) of Digoxin, Predose (Digoxin) and up to 24 hours postdose on Days 7, 10, and 17|Pharmacokinetics: Time of Maximum Observed Drug Concentration (Tmax) of Digoxin, Predose (Digoxin) and up to 24 hours postdose on Days 7, 10, and 17 |
|
| Sponsor/Collaborators: |
Sponsor: Eli Lilly and Company
|
| Gender: |
ALL
|
| Age: |
ADULT, OLDER_ADULT
|
| Phases: |
PHASE1
|
| Enrollment: |
24
|
| Study Type: |
INTERVENTIONAL
|
| Study Designs: |
Allocation: NA|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
|
| Start Date: |
2011-09
|
| Completion Date: |
2011-11
|
| Results First Posted: |
2014-10-07
|
| Last Update Posted: |
2014-10-07
|
| Locations: |
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Daytona Beach, Florida, 32117, United States
|
| URL: |
https://clinicaltrials.gov/show/NCT01436201
|
