A Phase 2 interventional study of PBI4050 in Type 2 Diabetes and Metabolic Syndrome, sponsored by Liminal BioSciences Ltd.. Completed at 1 site in Canada. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-04-11.
Sponsored by Liminal BioSciences Ltd. · Phase 2, Interventional, and Treatment
This is a Phase 2, open-label, single-arm study of the safety and tolerability of PBI-4050 800 mg daily oral administration in type 2 diabetes patients with metabolic syndrome.
A total of 12 patients will initially be enrolled for study participation. A Data Safety Monitoring Board (DSMB) will continuously review data obtained from the 12 patients. When the 12 patients have completed at least one month of study treatment, the DSMB will meet and determine whether additional patients may be enrolled or the study should be stopped. If the safety is deemed acceptable to continue with the study, the study will enroll a maximum of 36 patients.
This Phase 2 study will be performed by 1 site in Canada. The total duration of study participation for each patient is at least 18 weeks and comprises 6 study visits.
Patients who choose to participate in the extension study will be in the study for a total of up to 32 weeks.
10,925 studies on the registry are indexed under Diabetes Mellitus; 1,319 are open to participants now.
This study's enrollment of 24 is below the median of 80 across 8,367 interventional studies indexed under Diabetes Mellitus.
Browse Diabetes Mellitus studies →Liminal BioSciences Ltd. is the lead sponsor of 10 studies on the registry; none are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Four 200 mg capsules (total 800 mg) administered orally, once a day.
Drug: PBI4050
Number of subjects with abnormal laboratory values and/or adverse events that are related to treatment
Time frame: 7 months
Change from baseline on waist circumference
Time frame: 6 months
Change from baseline on biomarkers
% reduction and/or increase of biomarkers
Time frame: 6 months
Change from baseline on antidiabetic treatment
Treatment discontinued, dosing change, and/or new medication added
Time frame: 6 months
Change from baseline on triglycerides
Time frame: 6 months
Change from baseline on BP
Time frame: 6 months
Change from baseline on HDL-C
Time frame: 6 Months
Change from baseline on fasting plasma glucose
Time frame: 6 months
This study is completed, as verified in Oct 2016. You cannot join it, but the record below documents what was studied.
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Liminal BioSciences Ltd.