A Comparative Study of KES524 in Patients With Obesity Disease

Obesity Clinical Trial

Official title:

A Double-Blind, Placebo-Controlled, Comparative Study of KES524 in Patients With Obesity Disease

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00165685
• Other study ID #: KES524-J081-161
• Status: Completed
• Phase: Phase 3
• First received: September 12, 2005
• Last updated: January 28, 2010
• Start date: July 2004
• Est. completion date: March 2007

Study information

• Verified date: January 2010
• Source: Eisai Inc.
• Contact: n/a
• Is FDA regulated: No
• Health authority: Japan: Ministry of Health, Labor and Welfare
• Study type: Interventional

Clinical Trial Summary

To investigate the efficacy and safety of KES524 in patients with obesity (visceral fat obesity with type 2 diabetes and dyslipidemia), a 52-week, double-blind, placebo-controlled comparative study is conducted. This study aims to examine superiority of KES524 to placebo by employing change and percent change in body weight (primary endpoints) and changes in proportion of subjects achieving ≧ 5% weight reduction, BMI, waist circumference, visceral fat area, subcutaneous fat area, V/S ratio by abdominal CT scan, HbA1c, TG and HDL-C (secondary endpoints).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 0
• Est. completion date: March 2007
• Est. primary completion date: March 2007
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 20 Years to 64 Years

Eligibility

Inclusion Criteria:

• Patients with ?25 kg/m2 of BMI at the start of the observation period

• Patients with visceral fat area ?100 cm2 measured with abdominal CT scan

• Patients with the following two health impairments:

1. Patients with previously diagnosed type 2 diabetes and HbA1c between ?6.1% and <9.0% at the start of observation period

2. Patients with ?150 mg/dL of triglyceride (TG), and/or <40 mg/dL of high-density lipoprotein cholesterol (HDL-C) for serum lipid parameters as dyslipidemic index at the start of the observation period

• Patients continuously receiving diet therapy for 8 weeks or longer before the start of the observation period

• Patients not receiving antidiabetic (12 weeks), antihyperlipidemics (4 weeks) and/or antihypertensive (4 weeks) drugs. If used, those who have received a consistent dosage and administration beginning more than 4 weeks (more than 12 weeks for antidiabetics) before the start of the observation period

• Patients with ambulatory treatment aged between ?20 years and <65 years at the time of obtaining informed consent

• Patients who are given full explanation about the study objective and contents and can give written informed consent

Exclusion Criteria:

• Patients with pulse rate of ?100/min during the observation period

• Patients with systolic blood pressure of ?160 mmHg and/or with diastolic blood pressure of ?100 mmHg during the observation period

• Patients with body weight loss of ?3% as compared to that at the start of the observation period, or body mass index (BMI) that is reduced to <25 kg/m2 during the observation period

• Patients who have received insulin within 12 weeks before the start of the observation period

• Patients with present illness or past history of severe eating disorder (e.g., anorexia nervosa or bulimia nervosa)

• Patients with present illness or past history of drug allergy or severe allergic disease(s)

• Patients with present illness or past history of the following disorders:

• Coronary artery disease (myocardial infarction, angina), heart failure

• Serious diseases such as cardiovascular (severe tachycardiac heart failure), renal (renal failure), hepatic (severe hepatitis, cirrhosis), pancreatic (severe pancreatitis), psychotic (severe depression, schizophrenia, alcohol addict, drug addict) disorders

• Pregnant or lactating women, or women who intend to become pregnant during the study period

• Patients who previously participated in and were treated in another clinical study of KES524

• Patients who have received another study drug within 24 weeks before starting observation period of this study

• Patients who are judged to be ineligible for study entry by the investigator or subinvestigator

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Obesity

Intervention

Drug:
• Sibutramine Hydrochloride Monohydrate

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Eisai Limited

Country where clinical trial is conducted

Japan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change and percent change in body weight
Secondary	Proportion of subjects achieving ?5% weight reduction
Secondary	Change in BMI
Secondary	Change in waist circumference
Secondary	Change in visceral fat area, subcutaneous fat area, and V/S ratio by abdominal CT scan
Secondary	Change in HbA1c
Secondary	Change and percent change in fasting serum lipids (TG, HDL-C)