Absorption and Tolerability Studies of an Emulsion Containing the Coconut Oil-derived Glycerol Tridecanoate in Healthy Men
Primary Purpose
Polycystic Ovary Syndrome
Status
Withdrawn
Phase
Phase 1
Locations
Singapore
Study Type
Interventional
Intervention
Glyceryl Tridecanoate
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Polycystic Ovary Syndrome focused on measuring Safety, Tolerability, Pharmacokinetics, Absorption
Eligibility Criteria
Inclusion Criteria:
- Men
- 21 - 40 years of age
- Healthy as determined by medical, physical examination and clinical laboratory results
- Weigh at least 60 kg.
- Reliable and willing to follow study procedures.
- Able to read/ understand English
- Given written informed consent approved by NUS and the Ethical Review Board governing the site.
Exclusion Criteria:
- Known allergies to coconut oil, or related compounds,
- History or presence of cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, haematological, or neurological disorders capable of significantly altering the absorption, or metabolism or elimination of drugs or of constituting a risk when taking the study medication or interfering with the interpretation of data.
- History of drug abuse
- Evidence of hepatitis B infection
- Given a blood donation of more than 450 mL in the last 3 months or any blood donation within the last month.
- Intend to use over-the counter or prescription medication known to affect reproductive or metabolic functions (e.g. hormonal pills, metformin and etc.) including steroidal preparations or intend to use vitamin, mineral, herbal or dietary supplements or intend to consume GT health supplements during the study
- Participants will be advised to avoid consuming coconut oil, or palm oil or any food products/ health supplements containing any of these oils during the study and 3 days prior to the study.
Sites / Locations
- Investigational Medicine Unit, National University Health System
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Active
Placebo
Arm Description
Glyceryl Tridecanoate emulsion, single doses (5 g, 10 g, 20 g) to 3 cohorts
Sunflower oil emulsion, single doses (5 g, 10 g, 20 g) to 3 cohorts
Outcomes
Primary Outcome Measures
Incidence and severity of adverse events/severe events
Incidence and severity of adverse events/serious adverse events based on history, physical examination and vital signs and clinical chemistry
Secondary Outcome Measures
Decanoic acid
Serum will be extracted from blood samples for measurement of decanoic acid using gas chromatography-mass spectrometry (GC/MS)
Full Information
NCT ID
NCT03255889
First Posted
August 13, 2017
Last Updated
December 5, 2017
Sponsor
National University Hospital, Singapore
1. Study Identification
Unique Protocol Identification Number
NCT03255889
Brief Title
Absorption and Tolerability Studies of an Emulsion Containing the Coconut Oil-derived Glycerol Tridecanoate in Healthy Men
Official Title
Absorption and Tolerability Studies of an Emulsion Containing the Coconut Oil-derived Glycerol Tridecanoate in Healthy Men
Study Type
Interventional
2. Study Status
Record Verification Date
December 2017
Overall Recruitment Status
Withdrawn
Why Stopped
Expiry of grant funding
Study Start Date
August 28, 2017 (Anticipated)
Primary Completion Date
September 24, 2017 (Anticipated)
Study Completion Date
March 28, 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National University Hospital, Singapore
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The primary aim of the study is to test safety and tolerance of oral intake of GT oil in the form of a non-diary based emulsion (10g of GT per emulsion) in healthy men. This will be a single center study, and the recruitment is expected to happen over a 1-2- month's period.
Detailed Description
Polycystic Ovarian Syndrome (PCOS) is a hormonal disorder contributing to infertility in women. PCOS is also associated with Insulin resistance (IR) occurring at a high incidence rate of 50-70%. IR is a condition in which your body loses sensitivity to insulin requiring higher levels of it to maintain normal glucose levels in blood which hormones production from ovaries. Studies have demonstrated that the prevalence of the metabolic syndrome which is a cluster of condition such as increased blood pressure, high blood sugar, excess body fat around the waist, and abnormal cholesterol in women with PCOS is significantly higher than that of the general population. Medications that improve insulin sensitivity, such as thiazolidinediones (TZDs) and Metformin, an insulin sensitizer have been used in treating women with PCOS. Metformin major side effects consist of nausea, vomiting and gastrointestinal distress. TZDs are withdrawn from the market due to their adverse effect profile, which includes liver toxicity, weight gain, swelling due to water retention and cardiovascular diseases. As current treatment options are inadequate, there is a clinical need to identify new treatment regimens with a reduced adverse effect profile to improve the management of PCOS and its related metabolic syndrome.
Glyceryl Tridecanoate (GT) is a medium chain triglyceride (MCT); a form of dietary fat, which has a long history of safe use in in foods, drugs, cosmetics, can even be provided via the veins in individuals requiring supplemental nutrition. Decanoic acid, also known as capric acid, occurs naturally in coconut oil (8 - 10%) and palm kernel oil (4%). Importantly, the published findings show that oral administration of GT, the triglyceride form of decanoic acid, can improve insulin sensitivity and storage and breakdown of fat in animal models of diabetes. Notably, in the investigators' recent findings, DA could reduce androgen production and alleviate PCOS like symptoms in a test-induced PCOS rat model. Hence, there is a high likelihood that GT can improve the management of PCOS without the undesirable side effects that are observed with the thiazolidinediones.
The primary aim of the study is to test safety and tolerance of oral intake of GT oil in the form of a non-diary based emulsion (10g of GT per emulsion) in healthy men. This will be a single center study, and the recruitment is expected to happen over a 1-2- month's period.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycystic Ovary Syndrome
Keywords
Safety, Tolerability, Pharmacokinetics, Absorption
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Active
Arm Type
Active Comparator
Arm Description
Glyceryl Tridecanoate emulsion, single doses (5 g, 10 g, 20 g) to 3 cohorts
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Sunflower oil emulsion, single doses (5 g, 10 g, 20 g) to 3 cohorts
Intervention Type
Drug
Intervention Name(s)
Glyceryl Tridecanoate
Other Intervention Name(s)
GT
Intervention Description
Glyceryl Tridecanoate (GT) is the triglyceride form of decanoic acid (DA), a C10 fatty acid. GT belongs to the class of medium chain triglycerides (MCT), which has been accepted as a Generally Recognized As Safe food product by FDA. Decanoic acid, also known as capric acid, occurs naturally in coconut oil (8 - 10%) and palm kernel oil (4%).
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Sunflower oil emulsion of equal calories.
Primary Outcome Measure Information:
Title
Incidence and severity of adverse events/severe events
Description
Incidence and severity of adverse events/serious adverse events based on history, physical examination and vital signs and clinical chemistry
Time Frame
8 to 10 days
Secondary Outcome Measure Information:
Title
Decanoic acid
Description
Serum will be extracted from blood samples for measurement of decanoic acid using gas chromatography-mass spectrometry (GC/MS)
Time Frame
3 months
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Men
21 - 40 years of age
Healthy as determined by medical, physical examination and clinical laboratory results
Weigh at least 60 kg.
Reliable and willing to follow study procedures.
Able to read/ understand English
Given written informed consent approved by NUS and the Ethical Review Board governing the site.
Exclusion Criteria:
Known allergies to coconut oil, or related compounds,
History or presence of cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, haematological, or neurological disorders capable of significantly altering the absorption, or metabolism or elimination of drugs or of constituting a risk when taking the study medication or interfering with the interpretation of data.
History of drug abuse
Evidence of hepatitis B infection
Given a blood donation of more than 450 mL in the last 3 months or any blood donation within the last month.
Intend to use over-the counter or prescription medication known to affect reproductive or metabolic functions (e.g. hormonal pills, metformin and etc.) including steroidal preparations or intend to use vitamin, mineral, herbal or dietary supplements or intend to consume GT health supplements during the study
Participants will be advised to avoid consuming coconut oil, or palm oil or any food products/ health supplements containing any of these oils during the study and 3 days prior to the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eu Leong Yong, MD & PhD
Organizational Affiliation
National University Hospital, Singapore
Official's Role
Principal Investigator
Facility Information:
Facility Name
Investigational Medicine Unit, National University Health System
City
Singapore
ZIP/Postal Code
117599
Country
Singapore
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Absorption and Tolerability Studies of an Emulsion Containing the Coconut Oil-derived Glycerol Tridecanoate in Healthy Men
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