Clinical Trials Directory

Trials / Terminated

TerminatedNCT00600743

Effect of a CCK-1R Agonist on Food Intake in Humans

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
40 (actual)
Sponsor
St. Luke's-Roosevelt Hospital Center · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The ultimate aim of this study is to test the hypothesis that the oral cholecystokinin (CCK) agonist GSKI181771X will reduce the size of a binge meal among individuals with Bulimia Nervosa. The study will be conducted in phases. First, an effective dose for reducing food intake, when normal subjects eat normally will be attained. Next, it will be determined whether intake at this dose is reduced in control subjects instructed to eat to capacity. If the dose is still effective compared to placebo, the same dose will be tested in patients with bulimia nervosa.

Detailed description

This study tests the hypothesis that an oral CCK antagonist GSKI181771X will reduce the size of a binge meal. It was intended to study the effects of increasing doses on antagonist on normal individuals to find an effective dose in a non-binge meal before moving to a binge meal. Once the effects of the antagonist on a binge meal were found, the compound would be used on patients with bulimia nervosa. However, the product expired and more was not available before the patients were tested. Data are presented for the normal participants who were instructed to eat normally, followed by a group that was instructed to binge eat. Comparisons were made between groups with different instructions and between binge and normal meals.

Conditions

Interventions

TypeNameDescription
DRUGGSKI181771X (CCK-1R agonist)Drug one trial vs placebo
BEHAVIORALInstructions to binge eatSubjects will be instructed to binge eat and will also be given either drug or placebo
BEHAVIORALInstructions to eat normallySubjects will be instructed to eat normally and will also be given either drug or placebo
DRUGPlaceboDrug one trial vs placebo

Timeline

Start date
2008-01-01
Primary completion
2009-02-01
Completion
2009-02-01
First posted
2008-01-25
Last updated
2017-04-28
Results posted
2017-04-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00600743. Inclusion in this directory is not an endorsement.