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Completed

NCT Number: NCT01917760

Pharmacokinetics Study of Gamma-aminobutyric Acid

The purpose of this study is to determine upon administering GABA orally to a person how it is absorbed, distributed, as well as the drug's pharmacological effects on the body such as glucose levels, serum C-peptide and/or insulin levels (referred to as pharmacokinetics/pharmacodynamics). We will conduct experiments in normal subjects to address these questions.

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Key information

Age range

19 year–40 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Endocrinology and Metabolism,Huashan hospital

Shanghai, Shanghai Municipality, 200040, China

About this study

Type 1 diabetes is an autoimmune disease resulting from the progressive loss of pancreatic insulin-secreting beta-cells. This consequently leads to a lack of insulin and elevation of blood sugar, namely hyperglycemia, which is a major cause for the development of diabetes and its acute or chronic complications. The current treatment for type 1 diabetes requires a life-long dependency on daily insulin injections, causing inconvenience and burden to patients. Drug-induced hypoglycemia is also common as it presents a major challenge in insulin therapy. Furthermore, although insulin therapy is lifesaving, it is not a cure as it neither reverses the progression of the disease nor prevents the development of serious complications associated with this disease. New treatments are urgently needed.

Recent studies have demonstrated that a natural chemical found in the brain, gamma-aminobutyric acid (GABA), which is also produced in large quantities by pancreatic beta-cells, has beta-cell regenerative and immunoregulatory effects. Importantly, GABA prevented and partially reversed diabetes in type 1 diabetes mouse models. It is important to address essential questions regarding the potential effects of GABA in diabetic patients in humans. Given the largely unknown mechanism of action of GABA in the pancreas, and the limited information on how GABA is absorbed, distributed and eliminated from the human body, we plan to examine these issues (referred to as pharmacokinetics/pharmacodynamics) in normal subjects.

The outcome of this study will provide useful information on the mechanism of action of GABA in human subjects.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Volunteers in good health condition between 19 and 40 years of age (inclusive) at the time of signing the informed consent.
  • Body mass index (BMI) between 18.5 and 24 kg/m2 (inclusive), with weight greater than 50 kg.
  • Not on any medication 2 weeks before screening.
  • No blood donation within 3 months before screening.
  • Must sign the informed consent. Note: Blood and biochemical tests must be normal during the screening. However, if the participant's test-results were beyond the normal range, the individual can still be recruited as long as the results do not affect the experiment.

Exclusion criteria

  • Abnormalities of physical examination, laboratory tests, or ECG in screening, which may influence the results of the study.
  • Previous or existing history of severe heart, liver, kidney, gastrointestinal, nervous system, mental, or metabolic abnormalities as well as other diseases which can affect drug absorption, circulation, metabolism, or excretion.
  • History of alcoholism, smoking, or drug abuse within the past 1 year.
  • Participation in any clinical drug study within the past 30 days.
  • Any definite or suspected allergy or family history of allergy to GABA or any other similar drugs.

Treatment and study plan

Primary outcomes

  1. pharmacokinetic characteristics of γ-aminobutyric acid (GABA)

    Time frame: baseline and up to 30 days

    The primary endpoint of this study is to obtain the pharmacokinetic characteristics of γ-aminobutyric acid (GABA), including:

    • Area under the plasma concentration-time curve from time 0 to the last quantifiable concentration (AUC0-t),
    • Area under the plasma concentration-time curve from time 0 extrapolated to infinity (AUC0-∞),
    • Maximum observed plasma concentration (Cmax),
    • Time to maximum plasma concentration (Tmax), and
    • Terminal elimination half-life in plasma (t½)

Secondary outcomes

  1. serological characteristics

    Time frame: baseline and up to 30 days

    plasma glucose levels, insulin, C-peptide and glucagon levels will be measured

Other outcomes

  1. Exploratory measures

    Time frame: baseline and up to 30 days

    plasma glucagon-like peptide-1 (GLP-1) and glycated serum protein (GSP)will be measured.

Sponsors and collaborators

Lead sponsor

Huashan Hospital

Other

Collaborators

  • Unity Health Toronto
  • University of Florida
  • University of Massachusetts, Worcester

Registry information

Official study title

The Pharmacokinetics of Gamma-aminobutyric Acid in Healthy Volunteers.

Acronym: GABA-PK

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
Aug 7, 2013
Registry last updated
Nov 2, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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