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CompletedNCT02562573Updated Apr 11, 2017

Study to Evaluate the Safety and Tolerability of PBI-4050 in Type 2 Diabetes Patients With Metabolic Syndrome

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

Phase
Phase 2
Study type
Interventional
Enrollment
24
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

03

In context

Diabetes Mellitus

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 →

Lead sponsor

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.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Patient is 18 years of age or older.
  2. Patient has signed written informed consent.
  3. Patient has a clinical diagnosis of type 2 diabetes mellitus with a hemoglobin A1c (HbA1c) level between 7% and 10%.
  4. Patient has been receiving stable antidiabetic therapy (oral agents with or without basal insulin given once daily in the evening) for a minimum of 3 months before the screening visit.
  5. Patient is able and willing to self-monitor blood glucose level at home.
  6. Patient has a body mass index (BMI) of at least 27 kg/m2.
  7. Patient has metabolic syndrome, having at least 3 of the 5 metabolic syndrome risk factors.

Exclusion criteria

Exclusion Criteria:

  1. Patient requires intensive insulin therapy (defined as more than basal insulin given once daily in the evening) in addition to oral hypoglycemic agents for blood glucose control.
  2. Patient has recent or on-going infection requiring systemic treatment with an anti-infective agent within 30 days before screening.
  3. Patient has had at least one episode of severe hypoglycemia in the past 12 months, defined as having a blood glucose level \< 3.0 mmol/L and/or requiring third party assistance to treat hypoglycemic episode.
  4. Patient has evidence of significant cardiovascular disease, including myocardial infarction, unstable angina, coronary bypass surgery, percutaneous transluminal coronary angioplasty (PTCA), congestive heart failure (New York Heart Association Class III-IV), stroke, or severe ischemic disease within 3 months before screening.
  5. Patient has uncontrolled hypertension with BP > 150/95 mm Hg.
  6. Patient has a diagnosis of rheumatic or inflammatory disease, such as rheumatoid arthritis (RA), polymyalgia rheumatic (PMR), inflammatory bowel disease (IBD); or other autoimmune or inflammatory disease such as systemic lupus erythematosus (SLE) or psoriasis.
  7. Patient is concurrently taking and plans to routinely continue taking anti-inflammatory medications, such as nonsteroidal anti-inflammatory drugs (NSAIDs) and corticosteroids, during the study.
  8. Patient is currently using weight loss medications.
  9. Patient has significantly elevated liver enzyme levels, defined as alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≥ 2.5 × upper limit of normal (ULN) or total bilirubin above ULN.
  10. Patient has a history of chronic alcohol or other substance abuse.
  11. Woman who is pregnant, breast-feeding, or planning a pregnancy during the course of the study.
  12. Woman of childbearing potential who is unwilling to use adequate birth control throughout the duration of the study.
  13. Patient has any condition that, in the investigator's opinion, is likely to interfere with study conduct and compliance.
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
24 participants (actual)

Study arms

  • Experimental
    PBI4050

    Four 200 mg capsules (total 800 mg) administered orally, once a day.

    Drug: PBI4050

Interventions

  • DrugPBI4050
06

What researchers measure

Primary outcomes

  1. Number of subjects with abnormal laboratory values and/or adverse events that are related to treatment

    Time frame: 7 months

Secondary outcomes

  1. Change from baseline on waist circumference

    Time frame: 6 months

  2. Change from baseline on biomarkers

    % reduction and/or increase of biomarkers

    Time frame: 6 months

  3. Change from baseline on antidiabetic treatment

    Treatment discontinued, dosing change, and/or new medication added

    Time frame: 6 months

  4. Change from baseline on triglycerides

    Time frame: 6 months

  5. Change from baseline on BP

    Time frame: 6 months

  6. Change from baseline on HDL-C

    Time frame: 6 Months

  7. Change from baseline on fasting plasma glucose

    Time frame: 6 months

07

Study locations

1 site
  • Edmonton, Alberta, Canada
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 11, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02562573
Lead sponsor
Liminal BioSciences Ltd.
Responsible party
Sponsor
First posted
Sep 29, 2015
Start date
May 2015
Primary completion
Nov 2016
Completion
Nov 2016
Last update
Apr 11, 2017

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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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