search
Back to results

A Study of the Safety and Effectiveness of JNJ-16269110 (R256918) in Overweight and Obese Patients

Primary Purpose

Obesity, Nutritional and Metabolic Diseases, Metabolic Diseases

Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
placebo
R256918
R256918
R256918
Sponsored by
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring Obesity, Overweight, Body Weight, Body Size, Nutritional and Metabolic Diseases

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Obese or overweight at screening defined as: BMI greater than or equal to 30 kg/m2 and <50 kg/m2 or BMI greater than or equal to 27 kg/m2 and <50 kg/m2 in the presence of controlled hypertension and/or treated or untreated dyslipidemia. For patients receiving antihypertensive and/or hypolipidemic medications, these should have been at a stable dosage for at least 2 months before the start of the run-in period. Controlled hypertension is defined as a diastolic blood pressure <100 mmHg and a systolic blood pressure <160 mmHg, in the presence of antihypertensive drug treatment. For patients who are not on lipid-lowering drugs, dyslipidemia is defined as LDL-C greater than or equal to 3.4 mmol/L (130 mg/dL), HDL C <1 mmol/L (40 mg/dL) for men or <1.3 mmol/L (50 mg/dL) for women, or triglycerides greater than or equal to 1.7 mmol/L (150 mg/dL)
  • A stable weight, i.e., increasing or decreasing not more than 5 kg in the 3 months before the start of the run-in period
  • Consumption of breakfast and dinner on a daily basis
  • Ability to swallow the intact capsule (17.5 mm in length and 9.1 mm in diameter) with water, as judged by e.g., the patients's history of having no difficulty with swallowing e.g., capsules or intact tablets
  • Fasting plasma glucose <7.0 mmol/L (126 mg/dL) at screening
  • Women must be postmenopausal or surgically incapable of childbearing or if sexually active, be practicing an effective method of birth control

Exclusion Criteria:

  • History of obesity with a known cause (e.g., Cushing's disease)
  • History of anorexia nervosa, bulimia, or binge-eating disorder
  • An established diagnosis of diabetes mellitus or treatment with glucose lowering prescription drugs at screening
  • Prior exposure or known contraindication or hypersensitivity to R256918
  • History of weight-reducing diet or receiving any drugs to treat obesity within the 3 months prior to screening
  • Treatment with any investigational drug or device within 1 month before the start of the run-in period
  • History or evidence of liver or renal impairment
  • History of HIV or presence of hepatitis C antibodies or positive hepatitis B serology
  • History of clinically significant gastro-intestinal disease
  • History of major gastro-intestinal surgery other than appendectomy or uncomplicated cholecystectomy
  • Previous gastric restrictive surgery or other surgical procedures to induce weight loss
  • Liposuction within the last 3 months before screening
  • Pregnant or nursing women, or women who plan to become pregnant during the study
  • History of significant cardiovascular disease or hypertension
  • Elevated levels of thyroid-stimulating hormone (TSH)
  • A significant change in smoking habits within 3 months of the start of the run-in period
  • Malignancy or a history of a malignancy within 5 years before the start of the run-in period, other than basal cell carcinomas of the skin or in situ cervical carcinoma
  • History of seizures or significant central nervous system-related disorders
  • History of significant psychiatric disorder, including, schizophrenia, or psychosis

Sites / Locations

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Placebo Comparator

Arm Label

001

002

003

004

Arm Description

R256918 5 mg capsule twice daily

R256918 10 mg capsule twice daily

R256918 15 mg capsule twice daily

placebo Placebo capsule twice daily

Outcomes

Primary Outcome Measures

Mean change in body weight from baseline to Week 12.

Secondary Outcome Measures

Changes in body weight, body mass index (BMI), body composition, blood pressure, glucose, intestinal hormone levels, beta cell function and lipid parameters.
Quality of Life scores on questionnaires.
Safety parameters monitored at each visit.

Full Information

First Posted
December 21, 2007
Last Updated
April 24, 2014
Sponsor
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
search

1. Study Identification

Unique Protocol Identification Number
NCT00622765
Brief Title
A Study of the Safety and Effectiveness of JNJ-16269110 (R256918) in Overweight and Obese Patients
Official Title
A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Dose-Ranging Study to Investigate the Safety and Efficacy of JNJ-16269110 in Overweight and Obese Subjects
Study Type
Interventional

2. Study Status

Record Verification Date
April 2014
Overall Recruitment Status
Completed
Study Start Date
November 2007 (undefined)
Primary Completion Date
June 2008 (Actual)
Study Completion Date
June 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study investigates the effectiveness and safety of 12 weeks of treatment with JNJ-16269110 (R256918), in overweight and obese patients. The primary measure of effectiveness is the change in body weight at a clinically relevant dosage level during treatment. Additional measures include body mass index (BMI), DEXA (dual X-ray absorptiometry which is a specialized x-ray test that measures body composition), fasting glucose, lipid levels, and blood pressure. Safety assessments performed during the trial include laboratory tests, vital sign measurements, and adverse event reporting.
Detailed Description
This is a randomized (assigned study drug by chance), double-blind (both the patient and investigator do not know whether patient is assigned to receive study drug or placebo), placebo-controlled study involving overweight and obese patients. Patients are randomized to one of 4 treatment groups and receive study drug or placebo for a period of 12 weeks. The study consists of 3 phases: a pretreatment phase (including a screening period of 1 week and a period prior to active treatment of 4 weeks), the treatment period of 12 weeks, and a posttreatment phase (consisting of a follow-up visit). Standardized nonpharmacologic therapy (individualized calorie deficit diets containing no more than 30% calories from fat and nutritional counseling) will be administered from Week 4 through the follow-up period. During the treatment period, patients visit the center every two weeks. On each visit, patients come to the clinic after 8 hours fasting. For effectiveness assessments, patients will be weighed and BMI calculated at each visit; waist and hip circumference and DEXA measurements (for body composition and fat mass analysis) will be performed at selected time points. Additional effectiveness assessments from a blood sample include levels of fasting hemoglobin type A1c (HbA1c), glucose, cholesterol, triglycerides, insulin, C-peptide, and gastrointestinal hormones. Insulin sensitivity and pancreas function are evaluated. Safety evaluations, including incidence of adverse events, clinical laboratory results, vital signs, and electrocardiograms, are performed during the study. Patients complete a questionnaire related to stomach/bowel symptoms (GI) throughout the study. Blood samples will also be drawn for an analysis of the subjects genes and an analyses of the body's handling of the study drug. The overall duration of the study for each patient is approximately 19 weeks. The study hypothesis is that treatment with JNJ-16269110 (R256918) will cause a change in body weight compared to placebo and will be well tolerated in overweight and obese patients. This hypothesis will be investigated at each dosage level to determine a clinically relevant dose. 5 mg capsules, 10 mg capsules, 15 mg capsules, or matching placebo capsules taken orally.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Nutritional and Metabolic Diseases, Metabolic Diseases, Nutrition Disorders, Overweight
Keywords
Obesity, Overweight, Body Weight, Body Size, Nutritional and Metabolic Diseases

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
321 (Actual)

8. Arms, Groups, and Interventions

Arm Title
001
Arm Type
Experimental
Arm Description
R256918 5 mg capsule twice daily
Arm Title
002
Arm Type
Experimental
Arm Description
R256918 10 mg capsule twice daily
Arm Title
003
Arm Type
Experimental
Arm Description
R256918 15 mg capsule twice daily
Arm Title
004
Arm Type
Placebo Comparator
Arm Description
placebo Placebo capsule twice daily
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
Placebo capsule twice daily
Intervention Type
Drug
Intervention Name(s)
R256918
Intervention Description
5 mg capsule twice daily
Intervention Type
Drug
Intervention Name(s)
R256918
Intervention Description
10 mg capsule twice daily
Intervention Type
Drug
Intervention Name(s)
R256918
Intervention Description
15 mg capsule twice daily
Primary Outcome Measure Information:
Title
Mean change in body weight from baseline to Week 12.
Time Frame
Baseline, 12 weeks
Secondary Outcome Measure Information:
Title
Changes in body weight, body mass index (BMI), body composition, blood pressure, glucose, intestinal hormone levels, beta cell function and lipid parameters.
Time Frame
12 weeks
Title
Quality of Life scores on questionnaires.
Time Frame
12 weeks
Title
Safety parameters monitored at each visit.
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Obese or overweight at screening defined as: BMI greater than or equal to 30 kg/m2 and <50 kg/m2 or BMI greater than or equal to 27 kg/m2 and <50 kg/m2 in the presence of controlled hypertension and/or treated or untreated dyslipidemia. For patients receiving antihypertensive and/or hypolipidemic medications, these should have been at a stable dosage for at least 2 months before the start of the run-in period. Controlled hypertension is defined as a diastolic blood pressure <100 mmHg and a systolic blood pressure <160 mmHg, in the presence of antihypertensive drug treatment. For patients who are not on lipid-lowering drugs, dyslipidemia is defined as LDL-C greater than or equal to 3.4 mmol/L (130 mg/dL), HDL C <1 mmol/L (40 mg/dL) for men or <1.3 mmol/L (50 mg/dL) for women, or triglycerides greater than or equal to 1.7 mmol/L (150 mg/dL) A stable weight, i.e., increasing or decreasing not more than 5 kg in the 3 months before the start of the run-in period Consumption of breakfast and dinner on a daily basis Ability to swallow the intact capsule (17.5 mm in length and 9.1 mm in diameter) with water, as judged by e.g., the patients's history of having no difficulty with swallowing e.g., capsules or intact tablets Fasting plasma glucose <7.0 mmol/L (126 mg/dL) at screening Women must be postmenopausal or surgically incapable of childbearing or if sexually active, be practicing an effective method of birth control Exclusion Criteria: History of obesity with a known cause (e.g., Cushing's disease) History of anorexia nervosa, bulimia, or binge-eating disorder An established diagnosis of diabetes mellitus or treatment with glucose lowering prescription drugs at screening Prior exposure or known contraindication or hypersensitivity to R256918 History of weight-reducing diet or receiving any drugs to treat obesity within the 3 months prior to screening Treatment with any investigational drug or device within 1 month before the start of the run-in period History or evidence of liver or renal impairment History of HIV or presence of hepatitis C antibodies or positive hepatitis B serology History of clinically significant gastro-intestinal disease History of major gastro-intestinal surgery other than appendectomy or uncomplicated cholecystectomy Previous gastric restrictive surgery or other surgical procedures to induce weight loss Liposuction within the last 3 months before screening Pregnant or nursing women, or women who plan to become pregnant during the study History of significant cardiovascular disease or hypertension Elevated levels of thyroid-stimulating hormone (TSH) A significant change in smoking habits within 3 months of the start of the run-in period Malignancy or a history of a malignancy within 5 years before the start of the run-in period, other than basal cell carcinomas of the skin or in situ cervical carcinoma History of seizures or significant central nervous system-related disorders History of significant psychiatric disorder, including, schizophrenia, or psychosis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Johnson & Johnson Pharmaceutical Research & Development, L.L. C. Clinical Trial
Organizational Affiliation
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Official's Role
Study Director
Facility Information:
City
Edegem
Country
Belgium
City
Liege
Country
Belgium
City
Frederiksberg C N/A
Country
Denmark
City
Hellerup N/A
Country
Denmark
City
Vipperroed
Country
Denmark
City
Helsinki
Country
Finland
City
Kuopio
Country
Finland
City
Berlin
Country
Germany
City
Dresden
Country
Germany
City
Heidelberg
Country
Germany
City
Amsterdam
Country
Netherlands
City
Hilversum
Country
Netherlands
City
Rotterdam
Country
Netherlands
City
Göteborg
Country
Sweden
City
Huddinge
Country
Sweden
City
Liverpool
Country
United Kingdom
City
London
Country
United Kingdom
City
Luton
Country
United Kingdom

12. IPD Sharing Statement

Links:
URL
http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_JNJ_6051&studyid=729&filename=CR011362_CSR.pdf
Description
A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Dose-Ranging Study to Investigate the Safety and Efficacy of JNJ-16269110 in Overweight and Obese Subjects

Learn more about this trial

A Study of the Safety and Effectiveness of JNJ-16269110 (R256918) in Overweight and Obese Patients

We'll reach out to this number within 24 hrs