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Efficacy and Safety of Cycloset® Compared With Placebo When Added to Metformin

Primary Purpose

Type 2 Diabetes

Status
Terminated
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Bromocriptine Mesylate
Sponsored by
VeroScience
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 2 Diabetes focused on measuring diabetes, diabetes mellitus

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Diagnosed with type 2 diabetes mellitus, for at least six months prior to screening.
  2. 18-75 years of age, inclusive.
  3. Male or if female, is either:

    • postmenopausal or
    • of childbearing potential and has used appropriate contraceptive methods
  4. Treated with a stable dose of metformin at least 3 months.
  5. Has not been treated with a sulfonylurea, thiazolidinedione, meglitinide, alpha-glucosidase inhibitor, or combination oral anti-diabetic therapy within 3 months prior to screening.
  6. Has not been on a regimen of lipid-lowering agents or if on such a regimen, it has been stable for a minimum of 6 weeks at screening.
  7. HbA1c value between ≥ 7.5% and < 11%, at screening (Visit 1) and Visit 3.
  8. Fasting plasma glucose measurement of ≤260 mg/dL at screening (Visit 1) and Visit 3.
  9. Fasting C-peptide value equal to or greater than the normal accepted minimum value (e.g. < 0.9 NG/ml).
  10. Stable body weight, i.e., not varying by > 10% for at least3 months prior to screening
  11. Body mass index (BMI) at screening of 25 kg/m2 to 42 kg/m2,inclusive.
  12. If treated for hypertension, the individual has been on stable therapy for 1 month prior to screening.

Exclusion Criteria:

  1. Prior exogenous insulin therapy as part of an outpatient diabetes treatment regimen.
  2. Type 1 diabetes mellitus
  3. Clinically significant history of cardiac disease or presence of cardiac disease, including MI, clinically significant arrhythmia, unstable angina pectoris, moderate to severe congestive heart failure, CABG, or angioplasty; or expected to require CABG or angioplasty during the study.
  4. Uncontrolled hypertension, defined as systolic blood pressure > 160 or diastolic blood pressure > 100 mmHg measured in sitting position at screening(Visit 1)

    Clinically significant history or presence of:

  5. Hepatic disease (i.e. impaired liver function, including having AST or ALT greater than three times the upper limit of normal)
  6. Renal disease (i.e. renal impairment with a serum creatinine ≥ 1.4 mg/dl)
  7. Central nervous system disease, including epilepsy
  8. CVA within the last 3 years.
  9. Less than 5 years remission from clinically significant malignancy.
  10. Major surgical operation within 3 months of screening.
  11. Organ transplantation.
  12. Evidence of acute or chronic illness including known or suspected HIV,HBV, or HCV infection.
  13. Currently abuses drugs or alcohol, including binge drinking, or history of abuse that in the investigator's opinion would cause the individual to be noncompliant.
  14. Regularly uses medications with addictive potential such as opiates,narcotics, tranquilizers, etc.
  15. Used drugs for weight loss, e.g., Xenical® (orlistat), Meridia® (sibutramine),Acutrim® (phenylpropanolamine), or similar over-the-counter medications within 3 months of screening.
  16. Known hypersensitivity to any components of the study drugs.
  17. Received any experimental drug or used an experimental device within 3 months of screening or will do so during the study.
  18. Has received unstable dose of fibric acid derivatives within 3 months of the screening.
  19. Requires regular use of systemic corticosteroids by oral, intravenous (IV),or intramuscular (IM) route, or regular use of potent, inhaled intranasal steroids that are known to have a high rate of systemic absorption.
  20. Prescription sympathomimetic drugs within 7 days of screening.
  21. Started therapy with an erectile dysfunction drug within 2 weeks prior to screening. The subject may not begin treatment with an erectile dysfunction drug during the study period; subjects previously taking erectile dysfunction drugs should do so only under medical supervision.
  22. Donated blood within 60 days of screening. Donation of blood also is prohibited during the study and for 30 days after completion of the study.
  23. Occupation that requires a rotation of shift work or working over night shifts.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Placebo Comparator

    Arm Label

    Bromocriptine Mesylate

    Placebo

    Arm Description

    Bromocriptine mesylate 0.8 mg

    Bromocriptine mesylate 0.8 mg matching placebo

    Outcomes

    Primary Outcome Measures

    Change in Baseline to End of Study in HbA1c
    Too few subjects were enrolled to assess outcome to pre-specified statistical power.

    Secondary Outcome Measures

    Fasting Plasma Glucose and Lipids
    Number of Serious Adverse Events Experienced by the Subjects

    Full Information

    First Posted
    February 27, 2007
    Last Updated
    April 26, 2016
    Sponsor
    VeroScience
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00441363
    Brief Title
    Efficacy and Safety of Cycloset® Compared With Placebo When Added to Metformin
    Official Title
    A Randomized, Double-Blind, Parallel-Group Trial to Assess the Efficacy and Safety of Cycloset® Compared With Placebo When Added to Metformin in Patients With Type 2 Diabetes Mellitus
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2016
    Overall Recruitment Status
    Terminated
    Why Stopped
    Failure to Recruit in a Timely manner
    Study Start Date
    February 2005 (undefined)
    Primary Completion Date
    February 2006 (Actual)
    Study Completion Date
    March 2006 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    VeroScience

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The purpose of this study is to investigate the efficacy and safety of Cycloset® and placebo when added to metformin monotherapy (at least 1000 mg/day for 3 months prior to screening) in persons with type 2 diabetes mellitus who are not adequately controlled on metformin therapy alone.
    Detailed Description
    In the previously conducted Phase III clinical trials, Cycloset® (up to a maximum dose of 4.8 mg/day), administered either as monotherapy or combined with sulfonylurea therapy, significantly reduced HbA1c, fasting and post-prandial glucose and fasting and post-prandial triglycerides in obese individuals with type 2 diabetes mellitus. Clinical studies that combined Cycloset® with metformin were not as part of the original Cycloset® clinical program because metformin was not commercially available in the United States at the time that the studies were initiated. The present study is designed to investigate the efficacy and safety of Cycloset® compared to placebo when added to metformin monotherapy in persons with type 2 diabetes mellitus who are not adequately controlled on metformin therapy alone. A sufficient number of individuals will be screened to enroll up to 326 subjects;approximately 276 subjects are expected to complete treatment through study termination (Week 26). The study population will consist of individuals currently treated with metformin, for at least 3 months prior to the study start. Subjects who have ever received exogenous insulin therapy as part of an outpatient diabetes treatment regimen are to be excluded, as are those taking oral anti-diabetic agents other than metformin within 3 months of screening (e.g., sulfonylureas, thiazolidinediones,alpha-glucosidase inhibitors, or meglitinides). Subjects may be male or female(surgically sterile, postmenopausal, or using appropriate contraceptive methods if of childbearing potential), age 18 to 75 years, inclusive, and are to have a screening HbA1c value of ≥ 7.5% and <11.0% and a screening body mass index (BMI) in the range of 25 kg/m2 to 42 kg/m2, inclusive.

    6. Conditions and Keywords

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

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    66 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Bromocriptine Mesylate
    Arm Type
    Active Comparator
    Arm Description
    Bromocriptine mesylate 0.8 mg
    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    Bromocriptine mesylate 0.8 mg matching placebo
    Intervention Type
    Drug
    Intervention Name(s)
    Bromocriptine Mesylate
    Other Intervention Name(s)
    Cycloset
    Intervention Description
    0.8 mg tablet
    Primary Outcome Measure Information:
    Title
    Change in Baseline to End of Study in HbA1c
    Description
    Too few subjects were enrolled to assess outcome to pre-specified statistical power.
    Time Frame
    up to 24 weeks
    Secondary Outcome Measure Information:
    Title
    Fasting Plasma Glucose and Lipids
    Time Frame
    up to 24 weeks
    Title
    Number of Serious Adverse Events Experienced by the Subjects
    Time Frame
    up to 24 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    75 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Diagnosed with type 2 diabetes mellitus, for at least six months prior to screening. 18-75 years of age, inclusive. Male or if female, is either: postmenopausal or of childbearing potential and has used appropriate contraceptive methods Treated with a stable dose of metformin at least 3 months. Has not been treated with a sulfonylurea, thiazolidinedione, meglitinide, alpha-glucosidase inhibitor, or combination oral anti-diabetic therapy within 3 months prior to screening. Has not been on a regimen of lipid-lowering agents or if on such a regimen, it has been stable for a minimum of 6 weeks at screening. HbA1c value between ≥ 7.5% and < 11%, at screening (Visit 1) and Visit 3. Fasting plasma glucose measurement of ≤260 mg/dL at screening (Visit 1) and Visit 3. Fasting C-peptide value equal to or greater than the normal accepted minimum value (e.g. < 0.9 NG/ml). Stable body weight, i.e., not varying by > 10% for at least3 months prior to screening Body mass index (BMI) at screening of 25 kg/m2 to 42 kg/m2,inclusive. If treated for hypertension, the individual has been on stable therapy for 1 month prior to screening. Exclusion Criteria: Prior exogenous insulin therapy as part of an outpatient diabetes treatment regimen. Type 1 diabetes mellitus Clinically significant history of cardiac disease or presence of cardiac disease, including MI, clinically significant arrhythmia, unstable angina pectoris, moderate to severe congestive heart failure, CABG, or angioplasty; or expected to require CABG or angioplasty during the study. Uncontrolled hypertension, defined as systolic blood pressure > 160 or diastolic blood pressure > 100 mmHg measured in sitting position at screening(Visit 1) Clinically significant history or presence of: Hepatic disease (i.e. impaired liver function, including having AST or ALT greater than three times the upper limit of normal) Renal disease (i.e. renal impairment with a serum creatinine ≥ 1.4 mg/dl) Central nervous system disease, including epilepsy CVA within the last 3 years. Less than 5 years remission from clinically significant malignancy. Major surgical operation within 3 months of screening. Organ transplantation. Evidence of acute or chronic illness including known or suspected HIV,HBV, or HCV infection. Currently abuses drugs or alcohol, including binge drinking, or history of abuse that in the investigator's opinion would cause the individual to be noncompliant. Regularly uses medications with addictive potential such as opiates,narcotics, tranquilizers, etc. Used drugs for weight loss, e.g., Xenical® (orlistat), Meridia® (sibutramine),Acutrim® (phenylpropanolamine), or similar over-the-counter medications within 3 months of screening. Known hypersensitivity to any components of the study drugs. Received any experimental drug or used an experimental device within 3 months of screening or will do so during the study. Has received unstable dose of fibric acid derivatives within 3 months of the screening. Requires regular use of systemic corticosteroids by oral, intravenous (IV),or intramuscular (IM) route, or regular use of potent, inhaled intranasal steroids that are known to have a high rate of systemic absorption. Prescription sympathomimetic drugs within 7 days of screening. Started therapy with an erectile dysfunction drug within 2 weeks prior to screening. The subject may not begin treatment with an erectile dysfunction drug during the study period; subjects previously taking erectile dysfunction drugs should do so only under medical supervision. Donated blood within 60 days of screening. Donation of blood also is prohibited during the study and for 30 days after completion of the study. Occupation that requires a rotation of shift work or working over night shifts.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Richard E Scranton, MD
    Organizational Affiliation
    VeroScience
    Official's Role
    Study Director

    12. IPD Sharing Statement

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    Efficacy and Safety of Cycloset® Compared With Placebo When Added to Metformin

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