An Investigational Drug Study in Obese (Considerably Overweight) Patients (0364-006)(COMPLETED)
This study has been completed.
Sponsor:
Merck
Information provided by:
Merck
ClinicalTrials.gov Identifier:
NCT00109148
First received: April 22, 2005
Last updated: January 23, 2012
Last verified: January 2012
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Purpose
The purpose of this study is to determine the safety and effectiveness of an investigational drug in patients with obesity (considerably overweight).
| Condition | Intervention | Phase |
|---|---|---|
|
Obesity |
Drug: MK0364 |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Treatment |
| Official Title: | A Study to Assess the Safety and Efficacy of MK0364 in Obese Patients |
Resource links provided by NLM:
Further study details as provided by Merck:
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Patients who are obese (considerably overweight) based on body mass index.
Exclusion Criteria:
- Patients with serious or unstable current or past medical conditions
Contacts and Locations
More Information
No publications provided by Merck
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Executive Vice President, Clinical and Quantitative Sciences, Merck Sharp & Dohme Corp |
| ClinicalTrials.gov Identifier: | NCT00109148 History of Changes |
| Other Study ID Numbers: | MK-0364-006, 2005_011 |
| Study First Received: | April 22, 2005 |
| Last Updated: | January 23, 2012 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by Merck:
|
Obesity and obesity-related medical conditions |
Additional relevant MeSH terms:
|
Obesity Overnutrition Nutrition Disorders |
Overweight Body Weight Signs and Symptoms |
ClinicalTrials.gov processed this record on May 22, 2013