Efficacy of Liraglutide Therapy in Patients With IPAA

PHASE2TerminatedINTERVENTIONAL
Enrollment

8

Participants

Timeline

Start Date

March 22, 2022

Primary Completion Date

October 16, 2023

Study Completion Date

October 16, 2023

Conditions
PouchitisIrritable Pouch Syndrome
Interventions
DRUG

Liraglutide Pen Injector

Treatment will be initiated at 0.6 mg per day for one week. The patient will be instructed to increase the dose to 1.2/day and 1.8 mg /day in week 2 and in week 3, respectively. From week 3 after the start of the drug until week 6 the patient will apply 1.8 mg/day liraglutide. In case of intolerance (e.g. occurrence of refractory nausea) at a higher dose (e.g. 1.8 mg daily, the highest dose in this trial) liraglutide can be reduced to the previous level.

DRUG

Placebo Pen Injector

Matching placebo pens used to administer normal saline in the same fashion as for liraglutide

Trial Locations (1)

27599

University of North Carolina, Chapel Hill

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Novo Nordisk A/S

INDUSTRY

lead

University of North Carolina, Chapel Hill

OTHER

NCT04763564 - Efficacy of Liraglutide Therapy in Patients With IPAA | Biotech Hunter | Biotech Hunter