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Assessing the PK and Effect on Glucose and GI Hormone Concentrations of Metformin Delayed-Release in Subjects With T2DM

Primary Purpose

Type 2 Diabetes Mellitus

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
EFB0027 (metformin delayed release)
EFB0026 (metformin immediate-release)
Sponsored by
Elcelyx Therapeutics, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Type 2 Diabetes Mellitus

Eligibility Criteria

19 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Is 19 to 70 (inclusive) years old at Visit 1 (Screening).
  2. Is diagnosed with Type 2 Diabetes Mellitus with

    • HbA1c between 6.0 to 9.5% (inclusive) for subjects managing their diabetes with:

      i. Diet and exercise alone, or ii. A stable regimen (minimum of 2 months at Visit 1) of metformin alone, or iii. A stable regimen (minimum of 2 months at Visit 1) of DPP-4 inhibitor alone, OR

    • HbA1c between 6.0 to 8.5% (inclusive) for subjects managing their diabetes with a stable (minimum of 2 months at Visit 1) combination regimen of metformin and DPP-4 inhibitors.
  3. Has serum creatinine below the upper limit of normal at Visit 1 and an estimated creatinine clearance above 80 using the Crockroft and Gault equation (CrCl = [(140 - age) x body weight in kg] / (serum creatinine x 72) x (0.85 for females) [ref. 3].
  4. Has a body mass index (BMI) of 25.0 to 40.0 kg/m^2 (inclusive) at Screening.
  5. Is male, or is female and meets all of the following criteria:

    • Not breastfeeding
    • Negative pregnancy test result (human chorionic gonadotropin, beta subunit) at Visit 1 (Screening) (not applicable to hysterectomized females)
    • Surgically sterile, postmenopausal, or if of childbearing potential, must practice and be willing to continue to practice appropriate birth control during the entire duration of the study
  6. Has a physical examination with no clinically significant abnormalities as judged by the investigator.
  7. Ability to understand and willingness to adhere to protocol requirements.
  8. If on chronic thyroid pharmacologic therapy, the dose must be stable for at least 3 months prior to Visit 1 (Screening), and must have thyroid-stimulating hormone (TSH) test result in normal range at Visit 1 (Screening).

Exclusion Criteria:

  1. Has a clinically significant medical condition that could potentially affect study participation and/or personal well-being, as judged by the investigator, including but not limited to the following conditions:

    • Hepatic disease
    • Renal disease
    • Gastrointestinal disease
    • Endocrine disorder except diabetes
    • Cardiovascular disease
    • Seizure disorder
    • Organ transplantation
    • Chronic infection
  2. Has any chronic disease requiring medication that has been adjusted in the past 90 days (subjects may take acute intermittent over-the-counter medications such as Tylenol, if needed).
  3. Has any drug treatment that affects gastric pH (prescription or over-the-counter), including any antacids or medications such as Rolaids or Pepcid within 2 days of Visit 1 (Screening).
  4. Has had major surgery of any kind within 6 months of Visit 1 (Screening).
  5. Has received a blood transfusion within 6 months of Visit 1 (Screening).
  6. Has a history of >5 kg weight change within 3 months of Visit 1 (Screening).
  7. Has clinical laboratory test (clinical chemistry, hematology, or urinalysis) abnormalities other than those expected in subjects with diabetes and judged by the investigator to be clinically significant at Visit 1 (Screening).
  8. Has physical, psychological, or historical finding that, in the investigator's opinion, would make the subject unsuitable for the study.
  9. Currently abuses drugs or alcohol or has a history of abuse that in the investigator's opinion would cause the individual to be noncompliant with study procedures.
  10. Has donated blood within 2 months of Visit 1 (Screening) or is planning to donate blood during the study.
  11. Has used insulin within 3 months of Visit 1 (Screening).
  12. Has received GLP-1 receptor agonists and/or thiazolidinedione treatment within 6 months of Visit 1 (Screening).
  13. Has known intolerance to metformin.
  14. Has received any investigational drug within 1 month (or five half-lives of the investigational drug, whichever is greater) of Visit 1 (Screening).
  15. Has known allergies or hypersensitivity to any component of study treatment.
  16. Is employed by Elcelyx Therapeutics, Inc (that is an employee, temporary contract worker, or designee of the company).
  17. Smokes more than 10 cigarettes per day, 2 cigars per day, or uses more than 1 can of smokeless tobacco per week.

Sites / Locations

  • Celerion, Inc.
  • Celerion, Inc.

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Experimental

Experimental

Experimental

Arm Label

1000 mg EFB0026 (metformin immediate-release)

1000 mg EFB0027 (metformin delayed-release)

500 mg EFB0027 (metformin delayed-release)

500 mg EFB0026 + 1000 mg EFB0027

Arm Description

BID

BID

BID

BID

Outcomes

Primary Outcome Measures

Area Under the Curve (0-t) of Plasma Metformin
Measures from the time of dosing (0 h) to the time of the last quantifiable concentration following dose administration. The dose of study medication was administered at t = -1 min relative to the start time of the standardized breakfast.
Change in Fasting Plasma Glucose
LS mean difference from Baseline (Day 1) to Day 5
Within Treatment Comparison Based on Ratios of AUCs of GLP-1
Within Treatment Comparison Based on Ratios of AUCs of PYY

Secondary Outcome Measures

Full Information

First Posted
August 23, 2012
Last Updated
August 12, 2016
Sponsor
Elcelyx Therapeutics, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT01677299
Brief Title
Assessing the PK and Effect on Glucose and GI Hormone Concentrations of Metformin Delayed-Release in Subjects With T2DM
Official Title
A Randomized, Crossover Study Assessing the Effects of pH 6.5 Enteric Coating of Metformin HCl Tablets on Pharmacokinetics and Changes in Circulating Glucose and Gastrointestinal Hormone Concentrations in Subjects With Type 2 Diabetes Mellitus
Study Type
Interventional

2. Study Status

Record Verification Date
August 2016
Overall Recruitment Status
Completed
Study Start Date
May 2012 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
September 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Elcelyx Therapeutics, Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will evaluate how EFB0027 and EFB0026 behave in subjects with type 2 diabetes mellitus. In addition, this study will compare the effects of EFB0027 and EFB0026 on circulating concentrations of glucose and gastrointestinal hormones in subjects with type 2 diabetes mellitus.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes Mellitus

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 1, Phase 2
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1000 mg EFB0026 (metformin immediate-release)
Arm Type
Active Comparator
Arm Description
BID
Arm Title
1000 mg EFB0027 (metformin delayed-release)
Arm Type
Experimental
Arm Description
BID
Arm Title
500 mg EFB0027 (metformin delayed-release)
Arm Type
Experimental
Arm Description
BID
Arm Title
500 mg EFB0026 + 1000 mg EFB0027
Arm Type
Experimental
Arm Description
BID
Intervention Type
Drug
Intervention Name(s)
EFB0027 (metformin delayed release)
Other Intervention Name(s)
Met DR
Intervention Description
Comparison of enteric-coating to assess effect on PK
Intervention Type
Drug
Intervention Name(s)
EFB0026 (metformin immediate-release)
Other Intervention Name(s)
Met IR, metformin, Glucophage
Intervention Description
Active comparator
Primary Outcome Measure Information:
Title
Area Under the Curve (0-t) of Plasma Metformin
Description
Measures from the time of dosing (0 h) to the time of the last quantifiable concentration following dose administration. The dose of study medication was administered at t = -1 min relative to the start time of the standardized breakfast.
Time Frame
Time points at which data were collected to create the area under the curve (0-t) for plasma metformin were: t = -0.08, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 10, and 11 h relative to the start time of the standardized breakfast.
Title
Change in Fasting Plasma Glucose
Description
LS mean difference from Baseline (Day 1) to Day 5
Time Frame
Change from Baseline (Day 1) to Day 5
Title
Within Treatment Comparison Based on Ratios of AUCs of GLP-1
Time Frame
Ratio of Day 5 to Baseline
Title
Within Treatment Comparison Based on Ratios of AUCs of PYY
Time Frame
Ratio of Day 5 to Baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Is 19 to 70 (inclusive) years old at Visit 1 (Screening). Is diagnosed with Type 2 Diabetes Mellitus with HbA1c between 6.0 to 9.5% (inclusive) for subjects managing their diabetes with: i. Diet and exercise alone, or ii. A stable regimen (minimum of 2 months at Visit 1) of metformin alone, or iii. A stable regimen (minimum of 2 months at Visit 1) of DPP-4 inhibitor alone, OR HbA1c between 6.0 to 8.5% (inclusive) for subjects managing their diabetes with a stable (minimum of 2 months at Visit 1) combination regimen of metformin and DPP-4 inhibitors. Has serum creatinine below the upper limit of normal at Visit 1 and an estimated creatinine clearance above 80 using the Crockroft and Gault equation (CrCl = [(140 - age) x body weight in kg] / (serum creatinine x 72) x (0.85 for females) [ref. 3]. Has a body mass index (BMI) of 25.0 to 40.0 kg/m^2 (inclusive) at Screening. Is male, or is female and meets all of the following criteria: Not breastfeeding Negative pregnancy test result (human chorionic gonadotropin, beta subunit) at Visit 1 (Screening) (not applicable to hysterectomized females) Surgically sterile, postmenopausal, or if of childbearing potential, must practice and be willing to continue to practice appropriate birth control during the entire duration of the study Has a physical examination with no clinically significant abnormalities as judged by the investigator. Ability to understand and willingness to adhere to protocol requirements. If on chronic thyroid pharmacologic therapy, the dose must be stable for at least 3 months prior to Visit 1 (Screening), and must have thyroid-stimulating hormone (TSH) test result in normal range at Visit 1 (Screening). Exclusion Criteria: Has a clinically significant medical condition that could potentially affect study participation and/or personal well-being, as judged by the investigator, including but not limited to the following conditions: Hepatic disease Renal disease Gastrointestinal disease Endocrine disorder except diabetes Cardiovascular disease Seizure disorder Organ transplantation Chronic infection Has any chronic disease requiring medication that has been adjusted in the past 90 days (subjects may take acute intermittent over-the-counter medications such as Tylenol, if needed). Has any drug treatment that affects gastric pH (prescription or over-the-counter), including any antacids or medications such as Rolaids or Pepcid within 2 days of Visit 1 (Screening). Has had major surgery of any kind within 6 months of Visit 1 (Screening). Has received a blood transfusion within 6 months of Visit 1 (Screening). Has a history of >5 kg weight change within 3 months of Visit 1 (Screening). Has clinical laboratory test (clinical chemistry, hematology, or urinalysis) abnormalities other than those expected in subjects with diabetes and judged by the investigator to be clinically significant at Visit 1 (Screening). Has physical, psychological, or historical finding that, in the investigator's opinion, would make the subject unsuitable for the study. Currently abuses drugs or alcohol or has a history of abuse that in the investigator's opinion would cause the individual to be noncompliant with study procedures. Has donated blood within 2 months of Visit 1 (Screening) or is planning to donate blood during the study. Has used insulin within 3 months of Visit 1 (Screening). Has received GLP-1 receptor agonists and/or thiazolidinedione treatment within 6 months of Visit 1 (Screening). Has known intolerance to metformin. Has received any investigational drug within 1 month (or five half-lives of the investigational drug, whichever is greater) of Visit 1 (Screening). Has known allergies or hypersensitivity to any component of study treatment. Is employed by Elcelyx Therapeutics, Inc (that is an employee, temporary contract worker, or designee of the company). Smokes more than 10 cigarettes per day, 2 cigars per day, or uses more than 1 can of smokeless tobacco per week.
Facility Information:
Facility Name
Celerion, Inc.
City
Tempe
State/Province
Arizona
ZIP/Postal Code
85283
Country
United States
Facility Name
Celerion, Inc.
City
Lincoln
State/Province
Nebraska
ZIP/Postal Code
68502
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
27216492
Citation
DeFronzo RA, Buse JB, Kim T, Burns C, Skare S, Baron A, Fineman M. Once-daily delayed-release metformin lowers plasma glucose and enhances fasting and postprandial GLP-1 and PYY: results from two randomised trials. Diabetologia. 2016 Aug;59(8):1645-54. doi: 10.1007/s00125-016-3992-6. Epub 2016 May 23.
Results Reference
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Assessing the PK and Effect on Glucose and GI Hormone Concentrations of Metformin Delayed-Release in Subjects With T2DM

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