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Efficacy of MK0557 in Combination With Sibutramine or Orlistat
This study has been completed.
First Received: September 19, 2007   No Changes Posted
Sponsored by: Merck
Information provided by: Merck
ClinicalTrials.gov Identifier: NCT00533481
  Purpose

Study medicine will be given alone, or in combination with either sibutramine or orlistat, to obese subjects to compare the effect on body weight over a six month period.


Condition Intervention Phase
Obesity
Drug: MK0557
Phase II

MedlinePlus related topics: Obesity
Drug Information available for: MK 0557
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Factorial Assignment, Safety/Efficacy Study

Further study details as provided by Merck:

Study Start Date: December 2003
Study Completion Date: December 2003
  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Men and women between the ages of 18-65 who are considered obese (have a body mass index between 30 and 43)

Exclusion Criteria:

  • Subject has high blood pressure or is taking any high blood pressure medicine
  • History of psychiatric disorder, stroke, or heart disease
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00533481

Sponsors and Collaborators
Merck
Investigators
Study Director: Medical Monitor Merck
  More Information

No publications provided

Study ID Numbers: 2007_615
Study First Received: September 19, 2007
Last Updated: September 19, 2007
ClinicalTrials.gov Identifier: NCT00533481     History of Changes
Health Authority: United States: Food and Drug Administration

Study placed in the following topic categories:
Sibutramine
Body Weight
Signs and Symptoms
Obesity
Orlistat
Nutrition Disorders
Overweight
Overnutrition

Additional relevant MeSH terms:
Body Weight
Signs and Symptoms
Obesity
Nutrition Disorders
Overweight
Overnutrition

ClinicalTrials.gov processed this record on May 07, 2009