The Effect of Liraglutide on the Treatment of Coronary Artery Disease and Type 2 Diabetes

PHASE4CompletedINTERVENTIONAL
Enrollment

41

Participants

Timeline

Start Date

May 31, 2012

Primary Completion Date

October 31, 2014

Study Completion Date

July 31, 2015

Conditions
Coronary Artery DiseaseDiabetes Mellitus, Type 2
Interventions
DRUG

Liraglutide

Liraglutide injection pen is administered by the participant once daily by subcutaneous injection. It is given independent of meals. The starting dose is 0.6 mg. After 2 weeks the dose will be increased to 1.2 mg. The dose will be further increased after 4 weeks to 1.8 mg. After a total of 12 weeks of treatment, a wash-out period of 2 weeks follows. Subsequently, the participant will be crossed over to a second period of 12 weeks of treatment with placebo.

DRUG

Placebo

Volume-matched placebo injection pen is administered by the participant once daily by subcutaneous injection. It is given independent of meals. The starting dose is 0.6 mg volume-matched placebo. After 2 weeks the dose will be increased to 1.2 mg. The dose will be further increased after 4 weeks to 1.8 mg. After a total of 12 weeks of treatment, a wash-out period of 2 weeks follows. Subsequently, the participant will be crossed over to a second period of 12 weeks of treatment with liraglutide.

Trial Locations (1)

2400

Copenhagen University Hospital, Bispebjerg, Copenhagen

All Listed Sponsors
lead

Haugaard, Steen Bendix, M.D., DMSc

INDIV

NCT01595789 - The Effect of Liraglutide on the Treatment of Coronary Artery Disease and Type 2 Diabetes | Biotech Hunter | Biotech Hunter