NCT Number: NCT00482196
To Study Different Levels of MK0493 for Safety, Efficacy, and Tolerability in Obese Patients (0493-017)(COMPLETED)
To study different doses of MK0493 for safety, efficacy and tolerability in obese patients.
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Notify MeKey information
Conditions
Age range
21 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Patient is between 21 and 65 years of age
Exclusion criteria
- HIV positive as determined by medical history
- Patient is pregnant, lactating or plans to become pregnant
- Patient has undergone surgical treatment for obesity
- Patient has undergone a surgical procedure within 4 weeks prior to Visit 1 or plans to undergo a surgical procedure during the study
- Patient plans to consume more than 2 glasses of grapefruit juice per day during the study
- Patient has participated in another clinical study (involving an investigational drug) within 3 months prior to restudy screening
Treatment and study plan
Sponsors and collaborators
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Registry information
Important dates
- Study start
- 2005
- Primary completion
- 2006
- Study completion
- 2006
- First posted
- Jun 5, 2007
- Registry last updated
- Apr 28, 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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