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Completed

NCT Number: NCT01507038

Safety and Efficacy of YH14617 in Diabetes Mellitus

The objective of this study is to assess the safety, efficacy and pharmacokinetic of YH14617 after once weekly or biweekly injection in patients with type 2 Diabetes Mellitus to investigate the optimal recommended dosage. Study period is 20 weeks including 12 weeks of treatment period and 8weeks of follow-up period without treatment.

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Key information

Age range

20 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Yuhan

Seoul, South Korea

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Have signed a written informed consent voluntary, prior to the any procedure
  • Volunteers of aged between 20 years to 75 years
  • Have been diagnosed with type 2 diabetes at least 3 months prior to study
  • Have a body mass index (BMI) of > 23kg/m2 and have a history of stable body weight during 3 months prior to the first administration (not varying by > 5% in weight)
  • Have been treated with stable dose regimen of Metformin > 1500mg/day or maximum tolerant dose for at least 3 months prior to the first administration
  • Have an HbA1c between 7% and 10% inclusive

Exclusion criteria

  • Have been treated with insulin, sulfonylurea, thiazolidinedione class hypoglycemic drugs, exenatide or other GLP-1 receptor agonist, DPP4-inhibitor, glucocorticoid and drugs that promote weight loss within 3 months prior to the first administration
  • Have acute disease, other untreated disease or diabetic complications that needs additional treatment
  • Have severe renal disorder(serum creatinine concentration > 1.5 times of normal upper limit) or liver disorder(liver enzyme > 2 times of normal upper limit)
  • Have blood pressure > 160/100mmHg
  • Have been hospitalized due to cardiac disorder(angina, cardiac infarction, heart failure and etc.) within 1 year prior to the first administration
  • Have history of critical disease within 1 year prior to the first administration
  • Have untreated malignant tumor or have history of significant malignant tumor within 5 years prior to the first administration
  • Have fasting plasma glucose(FPG) > 250mg/dl or have random glucose level > 350mg/dl
  • Have more than 1 history of severe hypoglycemia that needed others help within 3 months prior to the first administration
  • Have a known allergy or hypersensitivity to drugs
  • Pregnant women, nursing mothers or subject who does not agree to assigned contraception in the study
  • Participated in any other clinical trials within 30 days prior to the first administration
  • Subject who is judged to be ineligible by principal investigator or sub-investigator according to various reasons other than above

Treatment and study plan

YH14617

Drug

1mg once weekly

Placebo

Drug

Once weekly

Primary outcomes

  1. Change from baseline in HbA1c at week 12

    Time frame: Baseline, Week 12

Secondary outcomes

  1. Change from baseline in body weight at week 12

    Time frame: Baseline, Week 12

  2. Change from baseline in fasting plasma glucose at week 12

    Time frame: Baseline, Week 12

  3. Change from baseline in 1,5-anhydroglucitol at week 12

    Time frame: Baseline, Week 12

Sponsors and collaborators

Lead sponsor

Yuhan Corporation

Industry

Collaborators

  • Peptron, Inc.

Registry information

Official study title

Phase II Clinical Trial to Investigate the Efficacy, Safety and Pharmacokinetics of YH14617 After Once Weekly or Biweekly Administration in Patients With Type 2 Diabetes Mellitus

Important dates

Study start
2011
Primary completion
2015
Study completion
2015
First posted
Jan 10, 2012
Registry last updated
Feb 18, 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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