Status:
COMPLETED
Effect of Cycloset on Glycemic Control When Added to Glucagon-like Peptide 1 (GLP-1) Analogue Therapy
Lead Sponsor:
The University of Texas Health Science Center at San Antonio
Collaborating Sponsors:
VeroScience
Conditions:
Type 2 Diabetes
Eligibility:
All Genders
30-69 years
Phase:
PHASE4
Brief Summary
Purpose This study will examine the effect of the addition of Cycloset upon glucose metabolism (glycemic control including post prandial glucose metabolism) in individuals with inadequately controlled...
Detailed Description
This is a single-site, prospective, cohort study that will assess the effect of Cycloset as add-on therapy in adult subjects with T2DM that is inadequately controlled (HbA1c 7.5% to 10.0%) on GLP-1 an...
Eligibility Criteria
Inclusion
- Type 2 diabetes male or female subjects between the ages of 30 and 70 years of age, inclusive, at Screening
- BMI = 24-40 kg/m2
- HbA1c = 7.5-10.0%
- Stable body weight (±3-4lbs) over the preceding 3 months
- Subjects currently receiving a stable dose of exenatide (2mg/week) or liraglutide (1.2-1.8 mg/day) for at least 90 days prior to determination of baseline HbA1C and eligibility for enrollment in the study protocol.
- Subjects with a daytime feeding/night time sleeping schedule
- Subjects with no evidence of major organ system disease as determined by physical exam, history, and screening laboratory data
- Women must be of non-childbearing potential as defined by one of the following:
- Women \>45 and \< 60 years of age at Screening, who have been amenorrheic for at least 2 years
- Women who have had a documented hysterectomy and/or bilateral oophorectomy
- Women \> 60 years of age
- Females of childbearing potential with a negative pregnancy test at Screening and Treatment visits, using one of the following forms of contraception for the duration of participation in the study (i.e., until Follow-up 7-14 days post last dose): Oral contraceptive, Injectable progesterone, subdermal implant, spermicidal foam/gel/film/cream/suppository, diaphragm with spermicide, copper or hormonal containing IUD (intrauterine device), sterile male partner vasectomized \> 6 month pre-dosing
- Evidence of a personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study
- Subjects must be willing and able to comply with scheduled visits, treatment, laboratory tests and study procedures.
Exclusion
- Recent (i.e., within three (3) months prior to Screening) evidence or medical history of unstable concurrent disease such as: documented evidence or history of clinically significant hematological, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, immunological, or clinically significant neurological disease.
- No history of T2DM
- BMI of less 24 and greater 40 kg/m2
- Unstable body weight (change of greater than ±3-4lbs over the preceding 3 months
- Subjects not currently receiving exenatide or liraglutide
- Subjects participating in an excessively heavy exercise program
- Subject with a feeding/sleeping schedule different from a daytime feeding/night time sleeping schedule
- Subjects taking medications known to alter glucose metabolism (with the exception of metformin and/or pioglitazone) or which effect brain neuro synaptic function are excluded.
- Subjects with evidence of major organ system disease as determined by physical exam, history, and screening laboratory data
- Pregnant subjects or subjects unwilling to use birth control during their study enrollment
- Blood donation of approximately 1 pint (500 mL) within 8 weeks prior to Screening 12. Subjects that are allergic to bromocriptine or any of the other ingredients in Cycloset, or take ergot medicines, breastfeeding or have history of syncope or Type 1 diabetes mellitus
- Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results that, in the judgment of the investigator, would make the subject inappropriate for entry into this study subjects of reproductive potential
Key Trial Info
Start Date :
June 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 30 2018
Estimated Enrollment :
23 Patients enrolled
Trial Details
Trial ID
NCT02299050
Start Date
June 1 2014
End Date
April 30 2018
Last Update
June 21 2019
Active Locations (1)
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1
University of Texas Health Science Center
San Antonio, Texas, United States, 78229