Clinical Trials Directory

Trials / Completed

CompletedNCT01262898

Dose Response of 28 Days of Dosing of GSK962040 in Type I and II Diabetic Male and Female Subjects With Gastroparesis

A Randomized, Double-Blind, Placebo-Controlled Multicenter Phase II Study to Evaluate the Safety and Efficacy and Dose Response of 28 Days of Once-Daily Dosing of the Oral Motilin Receptor Agonist GSK962040, in Type I and II Diabetic Male and Female Subjects With Gastroparesis

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
79 (actual)
Sponsor
GlaxoSmithKline · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

GSK962040 is a novel small molecule motilin agonist. The Phase I studies (MOT107043 and MOT109681) demonstrated that single doses of GSK962040 up to 150 mg and repeat dosing of up to 125 mg/day for 14 days were well tolerated with adverse events not occurring in greater prevalence than placebo, and no significant abnormal vital sign, ECG, or clinical laboratory findings. Pharmacokinetic parameters were linear and approximately dose proportional over the range of doses administered. Single doses of 50 mg - 150 mg GSK962040 significantly increased the rate of gastric emptying up to 40% as measured by the 13C octanoic acid stable isotope breath test. A similar effect of 50 mg and 125 mg on gastric emptying was observed throughout repeated dosing to healthy volunteers for 14-days. The aims of the present investigation (MOT114479) are to assess the pharmacodynamic effects (gastric emptying and symptoms), safety, tolerability, and pharmacokinetics of GSK962040 after 28 days of once-daily dosing in Type I and Type II diabetic subjects with gastroparesis. An additional aim is to characterize the dose/exposure - pharmacodynamic effect relationship.

Conditions

Interventions

TypeNameDescription
DRUGGSK962040 (5 mg tablet)5 mg tablet
DRUGGSK962040 (25 mg tablet)25 mg tablet
DRUGGSK962040 (125 mg tablet)125 mg tablet
DRUGPlacebomatching placebo tablet

Timeline

Start date
2011-05-03
Primary completion
2013-02-26
Completion
2013-02-26
First posted
2010-12-17
Last updated
2021-07-15
Results posted
2017-10-13

Locations

22 sites across 6 countries: United States, Australia, Belgium, Canada, Sweden, United Kingdom

Source: ClinicalTrials.gov record NCT01262898. Inclusion in this directory is not an endorsement.