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Completed

NCT Number: NCT01008163

A Dose-Finding, Efficacy and Safety Study of YY-351 in Patients With Type 2 Diabetes

The purpose of this trial is to determine the dosage selected and to evaluate the efficacy and safety of YY-351.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Seoul National University Bundang Hospital

Seongnam, Bungdang-Gu, 463-707, South Korea

About this study

Ginseng has been widely studied for treatment of diabetes, dyslipidemia and obesity. Interestingly, in addition to ginseng root, ginseng berry and leaf were also shown to reduce blood glucose in diabetic models. In our recent study, ginsam, vinegar extraction from Panax ginseng, which is enriched in the ginsenoside Rg3, has distinct beneficial effects on glucose metabolism and body weight control in an obese animal model of insulin resistance by changing the expression of genes involved in glucose and fatty acid metabolism. Our group has also published that Rg3 improves insulin signaling and glucose uptake primarily by stimulating the expression of IRS-1 and GLUT4. Thus, we have evaluated the efficacy, dose-response relationships and safety of a ginsam, a vinegar extract from Panax ginseng.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Previous diagnosis of Type 2 diabetes(more than 3months)
  • Patients aged over 18 years
  • FPG levels in the range : 126 - 270mg/dL or HbA1c : 7.0 - 12.0%

Exclusion criteria

  • Pregnant women, Breast feeding, or actively trying to be come pregnant
  • Patients with Type 1 DM, gestational diabetes or secondary diabetes
  • FPG levels in the range : ≥ 270mg/dL HbA1c : < 7.0, >12.0%
  • Patient who take the medicine which may affect to blood sugar control (i.e.systemic glucocorticoid)
  • Patients with diabetic complications or the history of a case that would affect to efficacy and safety evaluation (i.e. Thyroid disorder, Cushing's Syndrome, Multiple ovarian cystoma, pheochromocytoma)
  • Patients with Chronic hepatitis, hepatitis B, C (except healthy HBV carrier) or Liver diseases (AST or/and ALT >2 × ULN(upper limit normal))
  • Patients with Kidney disorder (Cr>2.0)

Treatment and study plan

YY-351/Placebo

Drug

comparison of different dosages of drug

Other names: Ginsam

YY-351

Drug

comparison of different dosages of drug

Other names: Ginsam

Placebo

Drug

comparison of different dosages of drug

Primary outcomes

  1. Change from baseline in the fasting plasma glucose and postprandial glucose [after 2 hours, oral glucose tolerance test (OGTT) (75 g)] and HbA1c

    Time frame: from baseline to Week 8

Secondary outcomes

  1. Subjects achieving a glycemic response defined as ≤ 7.0%

    Time frame: from baseline to Week 8

  2. Decrease of HbA1c > 0.5%

    Time frame: from baseline to Week 8

  3. Biomarkers [liver function tests (LFT), high-sensitivity C-reactive protein (hsCRP), adiponectin]

    Time frame: from baseline to Week 8

  4. Body weight (or body composition)

    Time frame: from baseline to Week 8

  5. Waist girth

    Time frame: from baseline to Week 8

  6. Homeostasis model assessment (HOMA)

    Time frame: from baseline to Week 8

  7. Lipid profile

    Time frame: from baseline to Week 8

Sponsors and collaborators

Lead sponsor

Yuyu Pharma, Inc.

Industry

Registry information

Official study title

A Phase Ⅱ, Randomized, Double-Blind, Placebo-Controlled, Dose-Finding, Efficacy and Safety of YY-351 in Patients With Type 2 Diabetes Mellitus

Important dates

Study start
2008
Primary completion
2009
Study completion
2009
First posted
Nov 4, 2009
Registry last updated
Feb 25, 2019

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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